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Indian Biosciences and Research Institute
Affiliation : Indian Educational and Research Society
Contact No : +91-9999 509892
Email : info@ibri.org.in
Website : www.ibri.org.in
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  •   Courses
  •   Reviews
  •   Contact
  •  QnA
Overview

About IBRI

Indian Biosciences and Research Institute is an autonomous institute dedicated to developing and nurturing the students and professionals through education, training, research and institute networking. IBRI is an unique organization as its Academic Board comprises of expertise professionals from the different domains like IT, Biotech, Pharmacy, Clinical Trials, Pharmacovigilance, Bioinformatics, life sciences, Biostatistics etc.

The institute was established to impart Competence, Comprehension, Course of Action and Character for Increased Employability and Earning value.

Why IBRI/Advantage IBRI

Top of the line IBRI advantage is its academic course-curriculum coupled with the recent trends and regulations as per global industries in different regions of the world.

The courses are designed to fill the gap of fresh students and what is desired in the industry by offering quality curriculum through the experienced faculties.

Apart from the students IBRI mission is to enhance the knowledgebase and skill sets of professionals with latest trends and updates like in regulatory, quality control and assurance, clinical trials, Pharmacovigilance, Bioinformatics and more….

The objectives of the imparting education in the applied life sciences fields of the institute is

  • To translate fundamental understanding into innovations in pharmaceutical sciences.
  • To create a successful model for global competitors and financially self-sustaining scientific research in India or abroad.

Admission Procedure

Admissions are open from time to time as per batch and the desirous/interested candidate for registration one has to submit completed prescribed Registration form. Steps for the submission of form are mentioned below:

  • Download the Registration form
  • Fill the Registration form in all respects and attach the requisite documents mentioned in the Registration form.
  • Pay requisite Registration fees along with Course Fees either by Draft or at par cheque drawn in the favour of Indian Biosciences and Research Institute payable at NOIDA. The fees can also be paid by cash
  • Submit the filled form along with all the documents by hand or Send it by Post or Courier at the address mentioned below
  • To
        The Program Coordinator,
        Indian Biosciences and Research Institute,
        C-50, First Floor, Sector-2,
        NOIDA 201301(UP)
        Mob No: 9999509892

Infrastructure

Classrooms
ibrs State of the art air conditioned class rooms enabled with audio visual systems creating a conducive environment for imparting quality teaching
Library
ibrs Amply satisfying intellectual appetite the library is well equipped with multiple copies of standard books by internationally acclaimed authors, national and international journals, periodicals,

Teaching and Research Laboratories

"I hear and I forget. I see and I remember. I do and I understand" - Confucius That's what we have labs for-most well equipped air conditioned laboratories with sophisticated latest state of the art instruments with cutting edge research expertise to provide hands-on training by best hands

Computer/Bioinformatics Lab

A hassle-free environment, with 24-hour high speed internet connectivity, N-Computing systems uninterrupted power supply, round the clock security, good maintenance of all equipment and central air-conditioning makes JBRI an ideal place for any motivated knowledge seeker. Staff and faculty (in-house and visiting) are all very accessible for help and advice. The friendly, congenial atmosphere makes working at IBRI a pleasure.

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Dean-Academics/Academics Consultant has been awarded many recognitions and awards from different agencies like Brands Academy, Times Media etc.

Placements/Summer Internship/Project Training

IBRI endows training in Bioinformatics/Biotechnology/Pharmacy in areas mentioned below

Bioinformatics
  • Agro-Informatics
  • Molecular Modelling
  • Phylogenetic Analysis
  • Computational Biology
  • in-silico Drug Designing
  • Biodiversity Informatics.
  • Database & Tool Development
  • Clinical Trials and Data Management
  • Structural and Functional Genomics
  • Waste Water Management (ETP/STP)
  • Micro Array Analysis and Probe Designing
  • Pharmacogenomics and more...........
Biotechnology
  • Basic Laboratory & Instrumentation
  • Microbiology Basic and Advanced
  • Proteomics
  • Biochemistry
  • HPLC
  • Chromatography
  • IPR
Pharmacy
  • Basic Laboratory & Instrumentation
  • HPLC
  • Chromatography
  • Herbal Quality Analysis
  • Basic Toxicology (I Level)
  • Advanced Toxicology (II Level)
  • Pharmacology/Pharmacokinetics/Pharmacodynamics
  • Histopathology
  • IPR
Clinical Trials and Data Management
  • Pharmacogenomics and more...........

Testimonials

ibrs

TEJASV TYAGI reviewed in the last week

Quality Very good

Hi, my name is Tejasva Pratap Tyagi and some of my friends who are doing Project Training in Bio-informatics told me that here at IBRI NOIDA they exploring new and advanced techniques in this science and so i recommend IBRI NOIDA for UG and PG students from Bio-informatics and Biotechnology background.

Kanvar Palreviewed 2 weeks ago

Quality Good

I am student of Janta Vedic College, Baraut (BAGHPAT) which affiliated by CCS University Meerut. There is a project in my 4th semester so joined IBRI NOIDA 11 April 2013, IBRI is Best institute for project training courses, all member of IBRI NOIDA is very supportive

Satyamvada Maurya reviewed 2 weeks ago

Quality Excellent

Hi, I am Satyamvada Maurya from Banasthali University,Jaipur,Rajasthan.I am doing MSc. Bioinformatics IV semester project at IBRI Noida. I joined ibri from January and i think its very good.I have learn lot of new things related to my field.My Project topic is "Development a tool for Gene Analysis".Abhinav Sir,Mithilesh Sir and Ajay Sir is very hard working and supportive. Infrastructure and the environment provided for working is excellent .So please if anyone interested in Bioinformatics training then join it.

Rahul Sharawat reviewed 3 weeks ago

Quality Good

IBRI, Noida and actually enjoying my project, learning every important lessions and softwares tools.......in an effective manner. I am glad to have our faculties.....Dr. Abhinav Srivastav (Director), Ajay sir, Mithilesh sir, and very supportive support members and so on. All our faculties are really well behaving, cooperative and supportive to clear any sort of confusions. The classses given by our Director sir and Ajay sir are very very informative and educative and will help us in future. The classes were really conceptual. I heartly, thank you IBRI to consider our 6 month project training on ''DRUG DESIGNING

Sonal Bhatia reviewed a month ago Quality Excellent

Hi i am sonal, student of Banasthali Vidyapeeth doing my MSc. final year project at IBRI Noida. I joined IBRI 3 months ago and I think its very good. Its a great way to excel in the field of dissertation and learn lot of new things related to your field. Faculty here is very hard working and supportive. Infrastructure and the environment provided for working is excellent. My project title is "In Silico Drug Designing and Database Development" and I am doing my work learning new things and with great experience. IBRI is simply 'THE BEST' and doing its work with excellence.

Hemant Singh reviewed 4 months ago Quality Excellent

I am Hemant Singh, student of M.Pharma (pharmacology) and I am doing project in IBRI nd my project topic is clinical trial and data management of drug 'A' on malaria. ryt nw my project is running in last phage nd my experience is very good in this institute. institute faculty is well qualified nd fully supportable with students so any one wants to good future thn join this institute. nd get better future for urself . thanks

A Google User reviewed 4 months ago Quality Very good

I join this institute from 7th jan. to 6th feb. for 1 month winter training. I learn some new technologies which was related to biotechnology.

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Students of 2012 Batch After completion Of Training

 

 

 

 

 

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Students of 2012 Batch during the Training

 

 

 

 

 

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Students of 2012 Batch Presented a Scenery to IBRI as a respect and for Quality Education imparted at IBRI

 

 

 

 

 

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2013 Batch pursuing Training

 

 

 

 

 

 

 

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Courses offered by Indian Biosciences and Research Institute All Courses 

Clinical Trials Data Management and Medical Writing

Other Medicine

Category: Other Medicine Certificate Courses

Degree: Certificate

Mode: Full Time

Medium: Campus

 

Read more..


Certificate Course in Biostatistics and Research Methodology

Other Medicine

Category: Other Medicine Certificate Courses

Degree: Certificate

Mode: Full Time

Medium: Campus

 

Read more..


Certificate Program in Regulatory Compliances and Affair

Category: Other Certificate Courses

Degree: Certificate

Mode: Correspondence

Medium: Distance Learning

Duration: 3 Months

 

Regulatory Affairs Courses - Mission: The Course Helps You To Fill In The Void Between The Curriculum Of A Theoretical Education And The Practical Demands Of Adhering To Pharmaceutical Regulatory.. Read more..


Certificate Course in Regulations for Biologics and Pharmaceutical Product

Pharmacy and Medicine

Category: DONOTUSE

Degree: Diploma

Mode: Correspondence

Medium: Distance Learning

Duration: 6 Months

 

Regulatory Affairs- Escalate Your Efficiency in Pharma Industry By Enrolling for Regulatory Affairs Course of IBRI NOIDA . Mission: The.. Read more..


Comprehensive Program in Regulatory Affairs for Pharmaceutics/Medical Diagnostics/Biologics

Other Medicine

Category: Other Post Graduate Diploma

Degree: PGD

Mode: Correspondence

Medium: Distance Learning

Duration: 1 Year

 

Regulatory Affairs- Escalate Your Efficiency in Pharma Industry By Enrolling for Regulatory Affairs Course of IBRI NOIDA . Mission: The.. Read more..


Name : Indian Biosciences and Research Institute
Location : C-50, First Floor, Sector-2
City : Noida
State : Uttar Pradesh
Country : India
Contact No : +91-9999 509892
Contact Email : info@ibri.org.in
Website : www.ibri.org.in 

Courses
Clinical Trials Data Management and Medical Writing
View Program Details
Category : Other Medicine Certificate Courses
Degree : Certificate
Mode : Full Time
Medium : Campus
Level : Certification

Certificate Course in Biostatistics and Research Methodology
View Program Details
Category : Other Medicine Certificate Courses
Degree : Certificate
Mode : Full Time
Medium : Campus
Level : Certification

Certificate Program in Regulatory Compliances and Affair
View Program Details
Category : Other Certificate Courses
Degree : Certificate
Mode : Correspondence
Medium : Distance Learning
Level : Certification

Regulatory Affairs Courses - Mission: The Course Helps You To Fill In The Void Between The Curriculum Of A Theoretical Education And The Practical Demands Of Adhering To Pharmaceutical Regulatory Compliance And Pharmaceutical Validation Processes. The pharmaceutical industry is financially strong and growing and developing rapidly. At all times, the industry needs to be able to recruit a sufficient number of professionals with a focused background in the pharmaceutical sciences.When a drug candidate is considered safe and effective on the basis of phase 3 trials, it must be approved internationally before being marketed. Regulatory Affairs is the area with a broad overview and the responsibility for collecting all data from the development processes and sending it to regulatory authorities where the trained people in regulatory affairs is required.The development of new drugs and medicinal products is a long and complicated process that starts with the glimmer of a new idea and ends with the effective marketing of a finished product i.e. the success is dependent on the approval by the authorities. Ever-changing laws and regulations are diving demand for regulatory affairs professionals who can help companies effectively bring medical products in market. To prepare you to effectively manage regulatory activities IBRI has designed three courses as per industry demand. Evaluation &Certification - Assignment based For more details like career prospects visit www.ibri.org.in

Certificate Course in Regulations for Biologics and Pharmaceutical Product
View Program Details
Category : DONOTUSE
Degree : Diploma
Mode : Correspondence
Medium : Distance Learning
Level : Diploma

Regulatory Affairs- Escalate Your Efficiency in Pharma Industry By Enrolling for Regulatory Affairs Course of IBRI NOIDA . Mission: The Course Helps You To Fill In The Void Between The Curriculum Of A Theoretical Education And The Practical Demands Of Adhering To Pharmaceutical Regulatory Compliance And Pharmaceutical Validation Processes. The pharmaceutical industry is financially strong and growing and developing rapidly. At all times, the industry needs to be able to recruit a sufficient number of professionals with a focused background in the pharmaceutical sciences. When a drug candidate is considered safe and effective on the basis of phase 3 trials, it must be approved internationally before being marketed. Regulatory Affairs is the area with a broad overview and the responsibility for collecting all data from the development processes and sending it to regulatory authorities where the trained people in Regulatory Affairs are required. The development of new drugs and medicinal products is a long and complicated process that starts with the glimmer of a new idea and ends with the effective marketing of a finished product i.e. the success is dependent on the approval by the authorities. Ever-changing laws and regulations are diving demand for regulatory affairs professionals who can help companies effectively bring medical products in market. To prepare you to effectively manage regulatory activities IBRI has designed the courses to fulfill the industry requirements. Course Highlights- Advantages of IBRI course: - IBRI course is different from other institutes and universities as its study material is based on recent trends and includes following topics: Procedure for the documents submission e.g.DMF,/E-CTD, Dossier Loan License( Contract Manufacturer) Hatch Waxmann Act; Bolar Provisions Separate Description of Regulations for Biologics, Medical Device/Pharmaceutics Recently globally included ofregulations and Compliance systems of Australia, Brazil. Biopharmaceuticals Market Authorization, Audits and inspections. Course Content- Paper I Introduction to Regulatory Affairs and Profession Paper II International Licensing and Drug Regulatory Affairs Paper III Regulatory Documentation for Biologics /Medical Diagnostics and Pharmaceutics (Submission of DMF, Dossiers etc.) Paper IV Global Regulatory Compliance Systems Evaluation &Certification - Assignment Based For more details like career prospects visit www.ibri.org.in

Comprehensive Program in Regulatory Affairs for Pharmaceutics/Medical Diagnostics/Biologics
View Program Details
Category : Other Post Graduate Diploma
Degree : PGD
Mode : Correspondence
Medium : Distance Learning
Level : PG

Regulatory Affairs- Escalate Your Efficiency in Pharma Industry By Enrolling for Regulatory Affairs Course of IBRI NOIDA . Mission: The Course Helps You To Fill In The Void Between The Curriculum Of A Theoretical Education And The Practical Demands Of Adhering To Pharmaceutical Regulatory Compliance And Pharmaceutical Validation Processes. The pharmaceutical industry is financially strong and growing and developing rapidly. At all times, the industry needs to be able to recruit a sufficient number of professionals with a focused background in the pharmaceutical sciences. When a drug candidate is considered safe and effective on the basis of phase 3 trials, it must be approved internationally before being marketed. Regulatory Affairs is the area with a broad overview and the responsibility for collecting all data from the development processes and sending it to regulatory authorities where the trained people in Regulatory Affairs are required. The development of new drugs and medicinal products is a long and complicated process that starts with the glimmer of a new idea and ends with the effective marketing of a finished product i.e. the success is dependent on the approval by the authorities. Ever-changing laws and regulations are diving demand for regulatory affairs professionals who can help companies effectively bring medical products in market. To prepare you to effectively manage regulatory activities IBRI has designed the courses to fulfill the industry requirements. Course Highlights- Advantages of IBRI course: - IBRI course is different from other institutes and universities as its study material is based on recent trends and includes following topics: Procedure for the documents submission e.g.DMF,/E-CTD, Dossier Loan License( Contract Manufacturer) Hatch Waxmann Act; Bolar Provisions Separate Description of Regulations for Biologics, Medical Device/Pharmaceutics Recently globally included ofregulations and Compliance systems of Australia, Brazil. Biopharmaceuticals Market Authorization, Audits and inspections. Course Content- Paper I Introduction to Regulatory Affairs and Profession Paper II International Licensing and Drug Regulatory Affairs Paper III Regulatory Documentation for Biologics /Medical Diagnostics and Pharmaceutics (Submission of DMF, Dossiers etc.) Paper IV Global Regulatory Compliance Systems Paper V Regulations for Clinical Trials, GMP, GLP and ICH Guidelines Paper V Regulatory Strategy and Quality Assurance Systems Paper VII Future of Biopharmaceuticals Paper VIII Research study Evaluation &Certification - Assignment Based For more details like career prospects visit www.ibri.org.in

Professional Designation in Medical and Scientific Documentation Writing
View Program Details
Category : Other Post Graduate Diploma
Degree : PGD
Mode : Correspondence
Medium : Distance Learning
Level : PG

Certificate Course in Medical and Scientific Documentation Writing The pharmaceutical and biotech industry is experiencing a sea change worldwide with more impetus on innovation and personalized medicine. The business models are maturing to the next level of niche busters and towards a coexistence of novel and the age old blockbuster strategies. With the economic drift and emerging economies like India, China, Brazil and Russia, the pharmaceutical and biotech industry is shifting research and development towards these regions especially in the phases of clinical development .Further, indigenous pharmaceutical and biotech companies in these regions are increasing their R&D efforts both for innovative molecules as well as genetic market. The course is designed to provide investigators with the concepts necessary to: Develop a protocol for a clinical trial that is fundable by a peer-reviewed agency Understand the statistical concepts necessary to design a clinical trial Understand the design and implementation issues unique to performing surgical trials Foster collaborative efforts necessary to conduct a clinical trial Certificate Course in Medical and Scientific Documentation Writing Paper-I: Basics of Good Medical Writing Paper-II: Scientific Writing: Concepts and Applications Paper-III: Protocol Writing for Clinical Trials Paper-IV: Case Report and Publication Writing Evaluation &Certification - Assignment based For more details of the course contact us- Program Coordinator IBRI NOIDA Mob: 9999509892, 0120-4122315 http://www.ibri.org.in/pdf/Course%20Stru_Clinical_Dista.pdf

Professional Designation in Clinical Trials
View Program Details
Category : Other Post Graduate Diploma
Degree : PGD
Mode : Correspondence
Medium : Distance Learning
Level : PG

Clinical Trials and Data Management Courses - The pharmaceutical and biotech industry is experiencing a sea change worldwide with more impetus on innovation and personalized medicine. The business models are maturing to the next level of niche busters and towards a coexistence of novel and the age old blockbuster strategies. With the economic drift and emerging economies like India, China, Brazil and Russia, the pharmaceutical and biotech industry is shifting research and development towards these regions especially in the phases of clinical development .Further, indigenous pharmaceutical and biotech companies in these regions are increasing their R&D efforts both for innovative molecules as well as genetic market. The course is designed to provide investigators with the concepts necessary to: develop a protocol for a clinical trial that is fundable by a peer-reviewed agency understand the statistical concepts necessary to design a clinical trial understand the design and implementation issues unique to performing surgical trials foster collaborative efforts necessary to conduct a clinical trial Evaluation &Certification - Assignment based For more details like career prospects visit www.ibri.org.in

Certificate Course in Clinical Trials Data Management
View Program Details
Category : Other Medicine Certificate Courses
Degree : Certificate
Mode : Correspondence
Medium : Distance Learning
Level : Certification

Clinical Trials and Data Management Courses - Conventional curative proceedings encompass medical professionals to determine remedy on the basis of the former attainments by self or others leading to the finest forecast of the likely course of a disease or ailment. There are concerns on that therapy is entirely persuasive and better room for promising amendments are determined with the help of Clinical Trials, which is cutting-edge operation in medicine and pharmaceutical research. Clinical Trial is a rigorously controlled test of a new drug or a new invasive medical device on human subjects; in the United States it is conducted under the direction of the FDA before being made available for general clinical use. Course Highlights- Paper-I: Introduction to Clinical Trials Data Management Paper-II: Biostatistics, SAS and Data Management Paper-III: Computerized Systems for E-Case Report Form and Data Acquisition and Validation Paper-IV: ICH, Ethics, IRB and Regulations for Clinical Trials Evaluation &Certification - Assignment based For more details like career prospects visit www.ibri.org.in

Comprehensive Program in Clinical Trials, Ethics and Regulations
View Program Details
Category : Other Post Graduate Diploma
Degree : PGD
Mode : Correspondence
Medium : Distance Learning
Level : PG

Clinical Trials and Data Management Courses - The pharmaceutical and biotech industry is experiencing a sea change worldwide with more impetus on innovation and personalized medicine. The business models are maturing to the next level of niche busters and towards a coexistence of novel and the age old blockbuster strategies. With the economic drift and emerging economies like India, China, Brazil and Russia, the pharmaceutical and biotech industry is shifting research and development towards these regions especially in the phases of clinical development .Further, indigenous pharmaceutical and biotech companies in these regions are increasing their R&D efforts both for innovative molecules as well as genetic market. The course is designed to provide investigators with the concepts necessary to: Develop a protocol for a clinical trial that is fundable by a peer-reviewed agency Understand the statistical concepts necessary to design a clinical trial Understand the design and implementation issues unique to performing surgical trials Foster collaborative efforts necessary to conduct a clinical trial Evaluation &Certification - Assignment based For more details like career prospects visit www.ibri.org.in

Certificate Course in Pharmacovigilance
View Program Details
Category : Other Medicine Certificate Courses
Degree : Certificate
Mode : Correspondence
Medium : Distance Learning
Level : Certification

Pharmacovigilance “Adding New Dimensions to Drug Discovery: Safety First” New Chemical Entities (NCE), high tech pharma products, vaccines as well as new dosage forms are being introduced in the country which throws up the challenge of monitoring Adverse Drug Reactions (ADRs) over a large population base. Pharmacovigilance focuses on adverse events, which is the science and activities relating to the detection, assessment, understanding and prevention of adverse effects or any other possible drug-related problems [WHO, 2002]. Consequently, the demand for qualified Pharmacovigilance & clinical research specialists has grown significantly with supply at present, not being able to match demand. With the advent of more pharmaceutical companies looking at India for their Pharmacovigilance activities, there is an imminent need to develop good professionals in Pharmacovigilance and there is ardent need of trained professionals in Pharmacovigilance. As Pharmacovigilance is becoming an important part of drug development as it deals with the patient’s safety keeping this in mind IBRI conducts courses in Pharmacovigilance along with the training of PV databases and software’s to regular batch students. Unique feature of the course is to learn to work software Vigiflow a tool used by all the industries today.(Regular Batch) As Pharmacovigilance and Clinical Research are becoming an important part of drug development as it deals with the patient’s safety keeping this in mind IBRI NOIDA has introduced certificate course in Pharmacovigilance. Paper-I: Principles of Pharmacovigilance Paper -II: Methodologies in Pharmacovigilance and Signal Detection Paper-III: Pharmacovigilance Compliance and Management Paper -IV: Pharmacovigilance Regulations and Guidelines Evaluation &Certification - Assignment Based For more details like career prospects contact us Program Co-ordinator Mob: 9999509892, Ph: 0120-4122315 visit http://www.ibri.org.in/Pharmacovigilance.aspx

Comprehensive Program in Clinical Trials Data Management & Pharmacovigilance
View Program Details
Category : Other Post Graduate Diploma
Degree : PGD
Mode : Correspondence
Medium : Distance Learning
Level : PG

Pharmacovigilance “Adding New Dimensions to Drug Discovery: Safety First” New Chemical Entities (NCE), high tech pharma products, vaccines as well as new dosage forms are being introduced in the country which throws up the challenge of monitoring Adverse Drug Reactions (ADRs) over a large population base. Pharmacovigilance focuses on adverse events, which is the science and activities relating to the detection, assessment, understanding and prevention of adverse effects or any other possible drug-related problems [WHO, 2002]. Consequently, the demand for qualified Pharmacovigilance & clinical research specialists has grown significantly with supply at present, not being able to match demand. With the advent of more pharmaceutical companies looking at India for their Pharmacovigilance activities, there is an imminent need to develop good professionals in Pharmacovigilance and there is ardent need of trained professionals in Pharmacovigilance. As Pharmacovigilance is becoming an important part of drug development as it deals with the patient’s safety keeping this in mind IBRI conducts courses in Pharmacovigilance along with the training of PV databases and software’s to regular batch students. Unique feature of the course is to learn to work software Vigiflow a tool used by all the industries today.(Regular Batch) Evaluation &Certification - Assignment based For more details like career prospects visit www.ibri.org.in

Certificate Course in Biopharmaceutical Quality Assurance and Control
View Program Details
Category : Other Medicine Certificate Courses
Degree : Certificate
Mode : Correspondence
Medium : Distance Learning
Level : Certification

Quality Assurance and Control including GMP, GLP Quality is an integral and vital component of any sampling and analysis effort. Both quality assurance (QA) and quality control (QC) are intended to insure data collected are adequate to fulfill project objectives and is of vital importance in Pharmaceutical industry where the quality parameters are very high and stringent. Quality assurance is a part of the overall management of the project, while quality control is the technical activity and documentation to pursue the quality objectives. This Program gives you a comprehensive knowledge of QA/QC starting from the beginning to advance level keeping in mind about the beginners and also about the present scenario in the pharmaceutical industry. Quality assurance (QA) is a wide-ranging concept covering all matters that individually or collectively influence the quality of a product. With regard to pharmaceuticals, quality assurance can be divided into four major areas: quality control, production, distribution, and inspections. The development of norms, standards and guidelines to promote quality assurance is an integral part of WHO’s Constitution and has been endorsed and supported through numerous World Health Assembly resolutions and more recently in those on WHO Medium-Term Strategic Plan for 2008-2015. At present the basis for designing or manufacturing of pharmaceutical products is QbD i.e. Quality by Design which is part of IBRI course curriculum . Evaluation &Certification - Assignment based For more details like career prospects visit www.ibri.org.in

Certificate Course in Good Manufacturing and Laboratory Practices
View Program Details
Category : Other Medicine Certificate Courses
Degree : Certificate
Mode : Correspondence
Medium : Distance Learning
Level : Certification

Quality Assurance and Control including GMP, GLP Quality is an integral and vital component of any sampling and analysis effort. Both quality assurance (QA) and quality control (QC) are intended to insure data collected are adequate to fulfill project objectives and is of vital importance in Pharmaceutical industry where the quality parameters are very high and stringent. Quality assurance is a part of the overall management of the project, while quality control is the technical activity and documentation to pursue the quality objectives. This Program gives you a comprehensive knowledge of QA/QC starting from the beginning to advance level keeping in mind about the beginners and also about the present scenario in the pharmaceutical industry. Quality assurance (QA) is a wide-ranging concept covering all matters that individually or collectively influence the quality of a product. With regard to pharmaceuticals, quality assurance can be divided into four major areas: quality control, production, distribution, and inspections. The development of norms, standards and guidelines to promote quality assurance is an integral part of WHO’s Constitution and has been endorsed and supported through numerous World Health Assembly resolutions and more recently in those on WHO Medium-Term Strategic Plan for 2008-2015. At present the basis for designing or manufacturing of pharmaceutical products is QbD i.e. Quality by Design which is part of IBRI course curriculum . Evaluation &Certification - Assignment based For more details like career prospects visit www.ibri.org.in

Comprehensive Program in GMP, Quality Assurance and Control Systems of Pharmaceutical Industry
View Program Details
Category : Other Post Graduate Diploma
Degree : PGD
Mode : Correspondence
Medium : Distance Learning
Level : PG

Quality Assurance and Control including GMP, GLP Quality is an integral and vital component of any sampling and analysis effort. Both quality assurance (QA) and quality control (QC) are intended to insure data collected are adequate to fulfill project objectives and is of vital importance in Pharmaceutical industry where the quality parameters are very high and stringent. Quality assurance is a part of the overall management of the project, while quality control is the technical activity and documentation to pursue the quality objectives. This Program gives you a comprehensive knowledge of QA/QC starting from the beginning to advance level keeping in mind about the beginners and also about the present scenario in the pharmaceutical industry. Quality assurance (QA) is a wide-ranging concept covering all matters that individually or collectively influence the quality of a product. With regard to pharmaceuticals, quality assurance can be divided into four major areas: quality control, production, distribution, and inspections. The development of norms, standards and guidelines to promote quality assurance is an integral part of WHO’s Constitution and has been endorsed and supported through numerous World Health Assembly resolutions and more recently in those on WHO Medium-Term Strategic Plan for 2008-2015. At present the basis for designing or manufacturing of pharmaceutical products is QbD i.e. Quality by Design which is part of IBRI course curriculum . Evaluation &Certification - Assignment based For more details like career prospects visit www.ibri.org.in

Certificate Course in Biostatistics and Research Methodology
View Program Details
Category : Other Medicine Certificate Courses
Degree : Certificate
Mode : Correspondence
Medium : Distance Learning
Level : Certification

Biostatistics and Research Methodology - The field of biostatistics has become an indispensable tool in improving our understanding of biological process and has a direct impact in ensuring the safety and efficacy of pharmacological and biotechnology products. In addition, the application of biostatistics is expanding to include several relatively new fields, such as medical imaging, ecological forecasting, and statistical genetics. The emphasis of the specialized certificate is in the application of statistical techniques to the analysis of life sciences data. Research is an integral part of the growth and expansion of sciences. It attempts to combine the on-going theoretical and conceptual debates and paradigms in various disciplines that contribute towards an understanding of issues relating to research methods in the context of development of the various methods adopted in research. Above brief introduction endows that the entire t subject’s areas biostatistics and research methodology are integral part of today’s biomedical and clinical research along with the genetics and public health. With the aim of filling the gap of knowledge of Biostatistics, &Research Methodology IBRI conducts and executes this specialized course with the help of experienced professionals. Evaluation &Certification - Assignment based Targeted Participants - This course is expected to be useful to researchers, trainers, administrators, policy makers, clinicians, pharmaceutical personnel and others affiliated with: Academic and higher educational institutions engaged in research pursuits Corporate sector and consultancy firms Government and public administration Civil society organisations Banks and other financial institutions and Other agencies undertaking research for policy formulation The credit points for the course are 45-50 Credits For more details like career prospects visit www.ibri.org.in

Certificate Course in Molecular and Human Genetics
View Program Details
Category : Other Medicine Certificate Courses
Degree : Certificate
Mode : Correspondence
Medium : Distance Learning
Level : Certification

Molecular and Human Genetics Molecular Genetics is a core discipline that is used by several cognate areas in modern biology including; cell biology, developmental biology, immunology, microbiology, neurobiology and physiology. It also underpins large areas of biotechnology. The molecular basis of human disease... Molecular Genetics is central to understanding the etiology of human disease and its diagnosis, prognosis and treatment. The rapidly evolving field of human genetics now incorporates genetic, biochemical, cell biological and developmental studies of both humans and model organisms to tackle biomedical problems important for human health and disease. Areas of study include both Mendelian and non-Mendelian hereditary diseases, genomics and mapping, Bioinformatics, developmental biology, neurogenetics, sex determination, cytogenetic, human malformation, and chromatin structure and function. Following the sequencing of the entire human genome, a wealth of resources is now available to researchers aiming to identify the genetic variants that influence human health. With this mission and vision of importance of Human and Molecular in Biomedical research and industry IBRI has introduced the course. This short term course is being conducted IBRI only which is also helpful for aspirants preparing for NET etc. A Course with a Difference for the students aspiring for UGC-NET, M.Sc./M.Tech Entrances/research Scholars/Scientists Targeted Participants: This course is expected to be useful to researchers, trainers, administrators, policy makers, clinicians, pharmaceutical personnel and others affiliated with: Academic and higher educational institutions engaged in research pursuits. Due to its trans-disciplinary nature, the course is open to students holding Bachelors degree in any branch of Science, Agriculture, Medicine, Pharmaceutics or Bioscience-related Technology/Engineering. Evaluation &Certification - Assignment based For more details like career prospects visit www.ibri.org.in

Professional Designation in Bioinformatics
View Program Details
Category : Other Post Graduate Diploma
Degree : PGD
Mode : Correspondence
Medium : Distance Learning
Level : PG

Bioinformatics Bioinformatics - Future of Biological Research 21st century is considered to be information technology era that has created an immense impact in every sphere of life leading to knowledge transfer i.e. outsourcing of information. Information is Knowledge and Today’s economy is Knowledge economy . Bioinformatics is a interdisciplinary subject between biological information and IT. Recent developments of the sciences have produced a wealth of experimental data of sequences and three-dimensional structures of biological macromolecules. With the advances of computer and information science, these data are available to the public from a variety of databases on the Internet. Bioinformatics has been defined as the science of examining the structure and function of genes and proteins through the use of computational analysis, statistics, and pattern recognition. A number of recent workforce studies have shown that there is a high current and unmet demand for people trained to various levels of expertise in bioinformatics, from technicians and technical librarians to developers of new and improved methodologies and applications. Bioinformatics is a rapidly evolving and developing field both in terms of breadth of scope of useful applications and in terms of depth of what can be accomplished. National estimates of needed positions in the field in the next four to five years are about 20,000. Bioinformatics: Key to Science and Technology's Future Evaluation &Certification - Assignment based For more details like career prospects visit www.ibri.org.in

Certificate Course in Applied Bioinformatics
View Program Details
Category : Other Medicine Certificate Courses
Degree : Certificate
Mode : Correspondence
Medium : Distance Learning
Level : Certification

Bioinformatics Bioinformatics - Future of Biological Research 21st century is considered to be information technology era that has created an immense impact in every sphere of life leading to knowledge transfer i.e. outsourcing of information. Information is Knowledge and Today’s economy is Knowledge economy . Bioinformatics is a interdisciplinary subject between biological information and IT. Recent developments of the sciences have produced a wealth of experimental data of sequences and three-dimensional structures of biological macromolecules. With the advances of computer and information science, these data are available to the public from a variety of databases on the Internet. Bioinformatics has been defined as the science of examining the structure and function of genes and proteins through the use of computational analysis, statistics, and pattern recognition. A number of recent workforce studies have shown that there is a high current and unmet demand for people trained to various levels of expertise in bioinformatics, from technicians and technical librarians to developers of new and improved methodologies and applications. Bioinformatics is a rapidly evolving and developing field both in terms of breadth of scope of useful applications and in terms of depth of what can be accomplished. National estimates of needed positions in the field in the next four to five years are about 20,000. Bioinformatics: Key to Science and Technology's Future Evaluation &Certification - Assignment based For more details like career prospects visit www.ibri.org.in

Comprehensive Program in Bioinformatics, Biological Databases and its Industrial Applications
View Program Details
Category : Other Post Graduate Diploma
Degree : PGD
Mode : Correspondence
Medium : Distance Learning
Level : PG

Bioinformatics Bioinformatics - Future of Biological Research 21st century is considered to be information technology era that has created an immense impact in every sphere of life leading to knowledge transfer i.e. outsourcing of information. Information is Knowledge and Today’s economy is Knowledge economy . Bioinformatics is a interdisciplinary subject between biological information and IT. Recent developments of the sciences have produced a wealth of experimental data of sequences and three-dimensional structures of biological macromolecules. With the advances of computer and information science, these data are available to the public from a variety of databases on the Internet. Bioinformatics has been defined as the science of examining the structure and function of genes and proteins through the use of computational analysis, statistics, and pattern recognition. A number of recent workforce studies have shown that there is a high current and unmet demand for people trained to various levels of expertise in bioinformatics, from technicians and technical librarians to developers of new and improved methodologies and applications. Bioinformatics is a rapidly evolving and developing field both in terms of breadth of scope of useful applications and in terms of depth of what can be accomplished. National estimates of needed positions in the field in the next four to five years are about 20,000. Bioinformatics: Key to Science and Technology's Future Evaluation &Certification - Assignment Based For more details like career prospects visit www.ibri.org.in

One Week Short Term Courses
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Category :
Degree :

Life Sciences, Biotech, Bioinformatics, Clinical Trials & Information Technology IBRI has introduced One Week Workshops for students to utilize their summer vacations in order to gear /train themselves for 21 st Century Knowledge-Led-Economy. The Workshops are on the topics/domains which will Increase Excellence for Breakthrough in Career Competency Earning Value. S.No Workshop On Duration Eligibility 1 Genomics & Proteomics One Week Graduate/PG/Professional 2 Next Generation Sequencing One Week Graduate/PG/Professional 3 Computer Aided Drug Designing & Cheminformatics One Week Graduate/PG/Professional 4 Human Genetics; Concepts, Methodology & Applications One Week Graduate/PG/Professional 5 Clinical Trials One Week Graduate/PG/Professional 6 Biostatistics & Research Methodology One Week Graduate/PG/Professional 7 Database Management Systems & Biological Database One Week Graduate/PG/Professional Computer Sciences Workshops One Week Graduate/PG/Professional 1 Information Technology: Basics One Week Graduate/PG/Professional 2 Database Management Systems One Week Graduate/PG/Professional 3 E- Commerce One Week Graduate/PG/Professional 4 C,C++, asp.net, Php, and more One Week Graduate/PG/Professional For more details like career prospects visit www.ibri.org.in

Certificate Course in Molecular and Human Genetics
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Category : Other Medicine Certificate Courses
Degree : Certificate
Mode : Full Time
Medium : Campus
Level : Certification

certificate course in Pharmacovigilance
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Category : Other Medicine Certificate Courses
Degree : Certificate
Mode : Full Time
Medium : Campus
Level : Certification

Master in Bioinformatics
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Category : Bioinformatics
Degree : M.Tech.
Mode : Full Time
Medium : Campus
Level : PG

M.Tech. Bioinformatics - Stands for Master of Technology in Bioinformatics. Typically, a M.Tech is a two year degree, minimum eligibility for which is a B.Tech. in Bioinformatics. Bio-Informatics is essentially the application of computer science and information technology to the field of molecular biology.

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Name : Indian Biosciences and Research Institute
Location : C-50, First Floor, Sector-2
City : Noida
State : Uttar Pradesh
Country : India
Contact No : +91-9999 509892
Contact Email : info@ibri.org.in
Website : www.ibri.org.in   
Courses
Clinical Trials Data Management and Medical Writing
View Program Details
Category : Other Medicine Certificate Courses
Degree : Certificate
Mode : Full Time
Medium : Campus
Level : Certification

Certificate Course in Biostatistics and Research Methodology
View Program Details
Category : Other Medicine Certificate Courses
Degree : Certificate
Mode : Full Time
Medium : Campus
Level : Certification

Certificate Program in Regulatory Compliances and Affair
View Program Details
Category : Other Certificate Courses
Degree : Certificate
Mode : Correspondence
Medium : Distance Learning
Level : Certification

Regulatory Affairs Courses - Mission: The Course Helps You To Fill In The Void Between The Curriculum Of A Theoretical Education And The Practical Demands Of Adhering To Pharmaceutical Regulatory Compliance And Pharmaceutical Validation Processes. The pharmaceutical industry is financially strong and growing and developing rapidly. At all times, the industry needs to be able to recruit a sufficient number of professionals with a focused background in the pharmaceutical sciences.When a drug candidate is considered safe and effective on the basis of phase 3 trials, it must be approved internationally before being marketed. Regulatory Affairs is the area with a broad overview and the responsibility for collecting all data from the development processes and sending it to regulatory authorities where the trained people in regulatory affairs is required.The development of new drugs and medicinal products is a long and complicated process that starts with the glimmer of a new idea and ends with the effective marketing of a finished product i.e. the success is dependent on the approval by the authorities. Ever-changing laws and regulations are diving demand for regulatory affairs professionals who can help companies effectively bring medical products in market. To prepare you to effectively manage regulatory activities IBRI has designed three courses as per industry demand. Evaluation &Certification - Assignment based For more details like career prospects visit www.ibri.org.in

Certificate Course in Regulations for Biologics and Pharmaceutical Product
View Program Details
Category : DONOTUSE
Degree : Diploma
Mode : Correspondence
Medium : Distance Learning
Level : Diploma

Regulatory Affairs- Escalate Your Efficiency in Pharma Industry By Enrolling for Regulatory Affairs Course of IBRI NOIDA . Mission: The Course Helps You To Fill In The Void Between The Curriculum Of A Theoretical Education And The Practical Demands Of Adhering To Pharmaceutical Regulatory Compliance And Pharmaceutical Validation Processes. The pharmaceutical industry is financially strong and growing and developing rapidly. At all times, the industry needs to be able to recruit a sufficient number of professionals with a focused background in the pharmaceutical sciences. When a drug candidate is considered safe and effective on the basis of phase 3 trials, it must be approved internationally before being marketed. Regulatory Affairs is the area with a broad overview and the responsibility for collecting all data from the development processes and sending it to regulatory authorities where the trained people in Regulatory Affairs are required. The development of new drugs and medicinal products is a long and complicated process that starts with the glimmer of a new idea and ends with the effective marketing of a finished product i.e. the success is dependent on the approval by the authorities. Ever-changing laws and regulations are diving demand for regulatory affairs professionals who can help companies effectively bring medical products in market. To prepare you to effectively manage regulatory activities IBRI has designed the courses to fulfill the industry requirements. Course Highlights- Advantages of IBRI course: - IBRI course is different from other institutes and universities as its study material is based on recent trends and includes following topics: Procedure for the documents submission e.g.DMF,/E-CTD, Dossier Loan License( Contract Manufacturer) Hatch Waxmann Act; Bolar Provisions Separate Description of Regulations for Biologics, Medical Device/Pharmaceutics Recently globally included ofregulations and Compliance systems of Australia, Brazil. Biopharmaceuticals Market Authorization, Audits and inspections. Course Content- Paper I Introduction to Regulatory Affairs and Profession Paper II International Licensing and Drug Regulatory Affairs Paper III Regulatory Documentation for Biologics /Medical Diagnostics and Pharmaceutics (Submission of DMF, Dossiers etc.) Paper IV Global Regulatory Compliance Systems Evaluation &Certification - Assignment Based For more details like career prospects visit www.ibri.org.in

Comprehensive Program in Regulatory Affairs for Pharmaceutics/Medical Diagnostics/Biologics
View Program Details
Category : Other Post Graduate Diploma
Degree : PGD
Mode : Correspondence
Medium : Distance Learning
Level : PG

Regulatory Affairs- Escalate Your Efficiency in Pharma Industry By Enrolling for Regulatory Affairs Course of IBRI NOIDA . Mission: The Course Helps You To Fill In The Void Between The Curriculum Of A Theoretical Education And The Practical Demands Of Adhering To Pharmaceutical Regulatory Compliance And Pharmaceutical Validation Processes. The pharmaceutical industry is financially strong and growing and developing rapidly. At all times, the industry needs to be able to recruit a sufficient number of professionals with a focused background in the pharmaceutical sciences. When a drug candidate is considered safe and effective on the basis of phase 3 trials, it must be approved internationally before being marketed. Regulatory Affairs is the area with a broad overview and the responsibility for collecting all data from the development processes and sending it to regulatory authorities where the trained people in Regulatory Affairs are required. The development of new drugs and medicinal products is a long and complicated process that starts with the glimmer of a new idea and ends with the effective marketing of a finished product i.e. the success is dependent on the approval by the authorities. Ever-changing laws and regulations are diving demand for regulatory affairs professionals who can help companies effectively bring medical products in market. To prepare you to effectively manage regulatory activities IBRI has designed the courses to fulfill the industry requirements. Course Highlights- Advantages of IBRI course: - IBRI course is different from other institutes and universities as its study material is based on recent trends and includes following topics: Procedure for the documents submission e.g.DMF,/E-CTD, Dossier Loan License( Contract Manufacturer) Hatch Waxmann Act; Bolar Provisions Separate Description of Regulations for Biologics, Medical Device/Pharmaceutics Recently globally included ofregulations and Compliance systems of Australia, Brazil. Biopharmaceuticals Market Authorization, Audits and inspections. Course Content- Paper I Introduction to Regulatory Affairs and Profession Paper II International Licensing and Drug Regulatory Affairs Paper III Regulatory Documentation for Biologics /Medical Diagnostics and Pharmaceutics (Submission of DMF, Dossiers etc.) Paper IV Global Regulatory Compliance Systems Paper V Regulations for Clinical Trials, GMP, GLP and ICH Guidelines Paper V Regulatory Strategy and Quality Assurance Systems Paper VII Future of Biopharmaceuticals Paper VIII Research study Evaluation &Certification - Assignment Based For more details like career prospects visit www.ibri.org.in

Professional Designation in Medical and Scientific Documentation Writing
View Program Details
Category : Other Post Graduate Diploma
Degree : PGD
Mode : Correspondence
Medium : Distance Learning
Level : PG

Certificate Course in Medical and Scientific Documentation Writing The pharmaceutical and biotech industry is experiencing a sea change worldwide with more impetus on innovation and personalized medicine. The business models are maturing to the next level of niche busters and towards a coexistence of novel and the age old blockbuster strategies. With the economic drift and emerging economies like India, China, Brazil and Russia, the pharmaceutical and biotech industry is shifting research and development towards these regions especially in the phases of clinical development .Further, indigenous pharmaceutical and biotech companies in these regions are increasing their R&D efforts both for innovative molecules as well as genetic market. The course is designed to provide investigators with the concepts necessary to: Develop a protocol for a clinical trial that is fundable by a peer-reviewed agency Understand the statistical concepts necessary to design a clinical trial Understand the design and implementation issues unique to performing surgical trials Foster collaborative efforts necessary to conduct a clinical trial Certificate Course in Medical and Scientific Documentation Writing Paper-I: Basics of Good Medical Writing Paper-II: Scientific Writing: Concepts and Applications Paper-III: Protocol Writing for Clinical Trials Paper-IV: Case Report and Publication Writing Evaluation &Certification - Assignment based For more details of the course contact us- Program Coordinator IBRI NOIDA Mob: 9999509892, 0120-4122315 http://www.ibri.org.in/pdf/Course%20Stru_Clinical_Dista.pdf

Professional Designation in Clinical Trials
View Program Details
Category : Other Post Graduate Diploma
Degree : PGD
Mode : Correspondence
Medium : Distance Learning
Level : PG

Clinical Trials and Data Management Courses - The pharmaceutical and biotech industry is experiencing a sea change worldwide with more impetus on innovation and personalized medicine. The business models are maturing to the next level of niche busters and towards a coexistence of novel and the age old blockbuster strategies. With the economic drift and emerging economies like India, China, Brazil and Russia, the pharmaceutical and biotech industry is shifting research and development towards these regions especially in the phases of clinical development .Further, indigenous pharmaceutical and biotech companies in these regions are increasing their R&D efforts both for innovative molecules as well as genetic market. The course is designed to provide investigators with the concepts necessary to: develop a protocol for a clinical trial that is fundable by a peer-reviewed agency understand the statistical concepts necessary to design a clinical trial understand the design and implementation issues unique to performing surgical trials foster collaborative efforts necessary to conduct a clinical trial Evaluation &Certification - Assignment based For more details like career prospects visit www.ibri.org.in

Certificate Course in Clinical Trials Data Management
View Program Details
Category : Other Medicine Certificate Courses
Degree : Certificate
Mode : Correspondence
Medium : Distance Learning
Level : Certification

Clinical Trials and Data Management Courses - Conventional curative proceedings encompass medical professionals to determine remedy on the basis of the former attainments by self or others leading to the finest forecast of the likely course of a disease or ailment. There are concerns on that therapy is entirely persuasive and better room for promising amendments are determined with the help of Clinical Trials, which is cutting-edge operation in medicine and pharmaceutical research. Clinical Trial is a rigorously controlled test of a new drug or a new invasive medical device on human subjects; in the United States it is conducted under the direction of the FDA before being made available for general clinical use. Course Highlights- Paper-I: Introduction to Clinical Trials Data Management Paper-II: Biostatistics, SAS and Data Management Paper-III: Computerized Systems for E-Case Report Form and Data Acquisition and Validation Paper-IV: ICH, Ethics, IRB and Regulations for Clinical Trials Evaluation &Certification - Assignment based For more details like career prospects visit www.ibri.org.in

Comprehensive Program in Clinical Trials, Ethics and Regulations
View Program Details
Category : Other Post Graduate Diploma
Degree : PGD
Mode : Correspondence
Medium : Distance Learning
Level : PG

Clinical Trials and Data Management Courses - The pharmaceutical and biotech industry is experiencing a sea change worldwide with more impetus on innovation and personalized medicine. The business models are maturing to the next level of niche busters and towards a coexistence of novel and the age old blockbuster strategies. With the economic drift and emerging economies like India, China, Brazil and Russia, the pharmaceutical and biotech industry is shifting research and development towards these regions especially in the phases of clinical development .Further, indigenous pharmaceutical and biotech companies in these regions are increasing their R&D efforts both for innovative molecules as well as genetic market. The course is designed to provide investigators with the concepts necessary to: Develop a protocol for a clinical trial that is fundable by a peer-reviewed agency Understand the statistical concepts necessary to design a clinical trial Understand the design and implementation issues unique to performing surgical trials Foster collaborative efforts necessary to conduct a clinical trial Evaluation &Certification - Assignment based For more details like career prospects visit www.ibri.org.in

Certificate Course in Pharmacovigilance
View Program Details
Category : Other Medicine Certificate Courses
Degree : Certificate
Mode : Correspondence
Medium : Distance Learning
Level : Certification

Pharmacovigilance “Adding New Dimensions to Drug Discovery: Safety First” New Chemical Entities (NCE), high tech pharma products, vaccines as well as new dosage forms are being introduced in the country which throws up the challenge of monitoring Adverse Drug Reactions (ADRs) over a large population base. Pharmacovigilance focuses on adverse events, which is the science and activities relating to the detection, assessment, understanding and prevention of adverse effects or any other possible drug-related problems [WHO, 2002]. Consequently, the demand for qualified Pharmacovigilance & clinical research specialists has grown significantly with supply at present, not being able to match demand. With the advent of more pharmaceutical companies looking at India for their Pharmacovigilance activities, there is an imminent need to develop good professionals in Pharmacovigilance and there is ardent need of trained professionals in Pharmacovigilance. As Pharmacovigilance is becoming an important part of drug development as it deals with the patient’s safety keeping this in mind IBRI conducts courses in Pharmacovigilance along with the training of PV databases and software’s to regular batch students. Unique feature of the course is to learn to work software Vigiflow a tool used by all the industries today.(Regular Batch) As Pharmacovigilance and Clinical Research are becoming an important part of drug development as it deals with the patient’s safety keeping this in mind IBRI NOIDA has introduced certificate course in Pharmacovigilance. Paper-I: Principles of Pharmacovigilance Paper -II: Methodologies in Pharmacovigilance and Signal Detection Paper-III: Pharmacovigilance Compliance and Management Paper -IV: Pharmacovigilance Regulations and Guidelines Evaluation &Certification - Assignment Based For more details like career prospects contact us Program Co-ordinator Mob: 9999509892, Ph: 0120-4122315 visit http://www.ibri.org.in/Pharmacovigilance.aspx

Comprehensive Program in Clinical Trials Data Management & Pharmacovigilance
View Program Details
Category : Other Post Graduate Diploma
Degree : PGD
Mode : Correspondence
Medium : Distance Learning
Level : PG

Pharmacovigilance “Adding New Dimensions to Drug Discovery: Safety First” New Chemical Entities (NCE), high tech pharma products, vaccines as well as new dosage forms are being introduced in the country which throws up the challenge of monitoring Adverse Drug Reactions (ADRs) over a large population base. Pharmacovigilance focuses on adverse events, which is the science and activities relating to the detection, assessment, understanding and prevention of adverse effects or any other possible drug-related problems [WHO, 2002]. Consequently, the demand for qualified Pharmacovigilance & clinical research specialists has grown significantly with supply at present, not being able to match demand. With the advent of more pharmaceutical companies looking at India for their Pharmacovigilance activities, there is an imminent need to develop good professionals in Pharmacovigilance and there is ardent need of trained professionals in Pharmacovigilance. As Pharmacovigilance is becoming an important part of drug development as it deals with the patient’s safety keeping this in mind IBRI conducts courses in Pharmacovigilance along with the training of PV databases and software’s to regular batch students. Unique feature of the course is to learn to work software Vigiflow a tool used by all the industries today.(Regular Batch) Evaluation &Certification - Assignment based For more details like career prospects visit www.ibri.org.in

Certificate Course in Biopharmaceutical Quality Assurance and Control
View Program Details
Category : Other Medicine Certificate Courses
Degree : Certificate
Mode : Correspondence
Medium : Distance Learning
Level : Certification

Quality Assurance and Control including GMP, GLP Quality is an integral and vital component of any sampling and analysis effort. Both quality assurance (QA) and quality control (QC) are intended to insure data collected are adequate to fulfill project objectives and is of vital importance in Pharmaceutical industry where the quality parameters are very high and stringent. Quality assurance is a part of the overall management of the project, while quality control is the technical activity and documentation to pursue the quality objectives. This Program gives you a comprehensive knowledge of QA/QC starting from the beginning to advance level keeping in mind about the beginners and also about the present scenario in the pharmaceutical industry. Quality assurance (QA) is a wide-ranging concept covering all matters that individually or collectively influence the quality of a product. With regard to pharmaceuticals, quality assurance can be divided into four major areas: quality control, production, distribution, and inspections. The development of norms, standards and guidelines to promote quality assurance is an integral part of WHO’s Constitution and has been endorsed and supported through numerous World Health Assembly resolutions and more recently in those on WHO Medium-Term Strategic Plan for 2008-2015. At present the basis for designing or manufacturing of pharmaceutical products is QbD i.e. Quality by Design which is part of IBRI course curriculum . Evaluation &Certification - Assignment based For more details like career prospects visit www.ibri.org.in

Certificate Course in Good Manufacturing and Laboratory Practices
View Program Details
Category : Other Medicine Certificate Courses
Degree : Certificate
Mode : Correspondence
Medium : Distance Learning
Level : Certification

Quality Assurance and Control including GMP, GLP Quality is an integral and vital component of any sampling and analysis effort. Both quality assurance (QA) and quality control (QC) are intended to insure data collected are adequate to fulfill project objectives and is of vital importance in Pharmaceutical industry where the quality parameters are very high and stringent. Quality assurance is a part of the overall management of the project, while quality control is the technical activity and documentation to pursue the quality objectives. This Program gives you a comprehensive knowledge of QA/QC starting from the beginning to advance level keeping in mind about the beginners and also about the present scenario in the pharmaceutical industry. Quality assurance (QA) is a wide-ranging concept covering all matters that individually or collectively influence the quality of a product. With regard to pharmaceuticals, quality assurance can be divided into four major areas: quality control, production, distribution, and inspections. The development of norms, standards and guidelines to promote quality assurance is an integral part of WHO’s Constitution and has been endorsed and supported through numerous World Health Assembly resolutions and more recently in those on WHO Medium-Term Strategic Plan for 2008-2015. At present the basis for designing or manufacturing of pharmaceutical products is QbD i.e. Quality by Design which is part of IBRI course curriculum . Evaluation &Certification - Assignment based For more details like career prospects visit www.ibri.org.in

Comprehensive Program in GMP, Quality Assurance and Control Systems of Pharmaceutical Industry
View Program Details
Category : Other Post Graduate Diploma
Degree : PGD
Mode : Correspondence
Medium : Distance Learning
Level : PG

Quality Assurance and Control including GMP, GLP Quality is an integral and vital component of any sampling and analysis effort. Both quality assurance (QA) and quality control (QC) are intended to insure data collected are adequate to fulfill project objectives and is of vital importance in Pharmaceutical industry where the quality parameters are very high and stringent. Quality assurance is a part of the overall management of the project, while quality control is the technical activity and documentation to pursue the quality objectives. This Program gives you a comprehensive knowledge of QA/QC starting from the beginning to advance level keeping in mind about the beginners and also about the present scenario in the pharmaceutical industry. Quality assurance (QA) is a wide-ranging concept covering all matters that individually or collectively influence the quality of a product. With regard to pharmaceuticals, quality assurance can be divided into four major areas: quality control, production, distribution, and inspections. The development of norms, standards and guidelines to promote quality assurance is an integral part of WHO’s Constitution and has been endorsed and supported through numerous World Health Assembly resolutions and more recently in those on WHO Medium-Term Strategic Plan for 2008-2015. At present the basis for designing or manufacturing of pharmaceutical products is QbD i.e. Quality by Design which is part of IBRI course curriculum . Evaluation &Certification - Assignment based For more details like career prospects visit www.ibri.org.in

Certificate Course in Biostatistics and Research Methodology
View Program Details
Category : Other Medicine Certificate Courses
Degree : Certificate
Mode : Correspondence
Medium : Distance Learning
Level : Certification

Biostatistics and Research Methodology - The field of biostatistics has become an indispensable tool in improving our understanding of biological process and has a direct impact in ensuring the safety and efficacy of pharmacological and biotechnology products. In addition, the application of biostatistics is expanding to include several relatively new fields, such as medical imaging, ecological forecasting, and statistical genetics. The emphasis of the specialized certificate is in the application of statistical techniques to the analysis of life sciences data. Research is an integral part of the growth and expansion of sciences. It attempts to combine the on-going theoretical and conceptual debates and paradigms in various disciplines that contribute towards an understanding of issues relating to research methods in the context of development of the various methods adopted in research. Above brief introduction endows that the entire t subject’s areas biostatistics and research methodology are integral part of today’s biomedical and clinical research along with the genetics and public health. With the aim of filling the gap of knowledge of Biostatistics, &Research Methodology IBRI conducts and executes this specialized course with the help of experienced professionals. Evaluation &Certification - Assignment based Targeted Participants - This course is expected to be useful to researchers, trainers, administrators, policy makers, clinicians, pharmaceutical personnel and others affiliated with: Academic and higher educational institutions engaged in research pursuits Corporate sector and consultancy firms Government and public administration Civil society organisations Banks and other financial institutions and Other agencies undertaking research for policy formulation The credit points for the course are 45-50 Credits For more details like career prospects visit www.ibri.org.in

Certificate Course in Molecular and Human Genetics
View Program Details
Category : Other Medicine Certificate Courses
Degree : Certificate
Mode : Correspondence
Medium : Distance Learning
Level : Certification

Molecular and Human Genetics Molecular Genetics is a core discipline that is used by several cognate areas in modern biology including; cell biology, developmental biology, immunology, microbiology, neurobiology and physiology. It also underpins large areas of biotechnology. The molecular basis of human disease... Molecular Genetics is central to understanding the etiology of human disease and its diagnosis, prognosis and treatment. The rapidly evolving field of human genetics now incorporates genetic, biochemical, cell biological and developmental studies of both humans and model organisms to tackle biomedical problems important for human health and disease. Areas of study include both Mendelian and non-Mendelian hereditary diseases, genomics and mapping, Bioinformatics, developmental biology, neurogenetics, sex determination, cytogenetic, human malformation, and chromatin structure and function. Following the sequencing of the entire human genome, a wealth of resources is now available to researchers aiming to identify the genetic variants that influence human health. With this mission and vision of importance of Human and Molecular in Biomedical research and industry IBRI has introduced the course. This short term course is being conducted IBRI only which is also helpful for aspirants preparing for NET etc. A Course with a Difference for the students aspiring for UGC-NET, M.Sc./M.Tech Entrances/research Scholars/Scientists Targeted Participants: This course is expected to be useful to researchers, trainers, administrators, policy makers, clinicians, pharmaceutical personnel and others affiliated with: Academic and higher educational institutions engaged in research pursuits. Due to its trans-disciplinary nature, the course is open to students holding Bachelors degree in any branch of Science, Agriculture, Medicine, Pharmaceutics or Bioscience-related Technology/Engineering. Evaluation &Certification - Assignment based For more details like career prospects visit www.ibri.org.in

Professional Designation in Bioinformatics
View Program Details
Category : Other Post Graduate Diploma
Degree : PGD
Mode : Correspondence
Medium : Distance Learning
Level : PG

Bioinformatics Bioinformatics - Future of Biological Research 21st century is considered to be information technology era that has created an immense impact in every sphere of life leading to knowledge transfer i.e. outsourcing of information. Information is Knowledge and Today’s economy is Knowledge economy . Bioinformatics is a interdisciplinary subject between biological information and IT. Recent developments of the sciences have produced a wealth of experimental data of sequences and three-dimensional structures of biological macromolecules. With the advances of computer and information science, these data are available to the public from a variety of databases on the Internet. Bioinformatics has been defined as the science of examining the structure and function of genes and proteins through the use of computational analysis, statistics, and pattern recognition. A number of recent workforce studies have shown that there is a high current and unmet demand for people trained to various levels of expertise in bioinformatics, from technicians and technical librarians to developers of new and improved methodologies and applications. Bioinformatics is a rapidly evolving and developing field both in terms of breadth of scope of useful applications and in terms of depth of what can be accomplished. National estimates of needed positions in the field in the next four to five years are about 20,000. Bioinformatics: Key to Science and Technology's Future Evaluation &Certification - Assignment based For more details like career prospects visit www.ibri.org.in

Certificate Course in Applied Bioinformatics
View Program Details
Category : Other Medicine Certificate Courses
Degree : Certificate
Mode : Correspondence
Medium : Distance Learning
Level : Certification

Bioinformatics Bioinformatics - Future of Biological Research 21st century is considered to be information technology era that has created an immense impact in every sphere of life leading to knowledge transfer i.e. outsourcing of information. Information is Knowledge and Today’s economy is Knowledge economy . Bioinformatics is a interdisciplinary subject between biological information and IT. Recent developments of the sciences have produced a wealth of experimental data of sequences and three-dimensional structures of biological macromolecules. With the advances of computer and information science, these data are available to the public from a variety of databases on the Internet. Bioinformatics has been defined as the science of examining the structure and function of genes and proteins through the use of computational analysis, statistics, and pattern recognition. A number of recent workforce studies have shown that there is a high current and unmet demand for people trained to various levels of expertise in bioinformatics, from technicians and technical librarians to developers of new and improved methodologies and applications. Bioinformatics is a rapidly evolving and developing field both in terms of breadth of scope of useful applications and in terms of depth of what can be accomplished. National estimates of needed positions in the field in the next four to five years are about 20,000. Bioinformatics: Key to Science and Technology's Future Evaluation &Certification - Assignment based For more details like career prospects visit www.ibri.org.in

Comprehensive Program in Bioinformatics, Biological Databases and its Industrial Applications
View Program Details
Category : Other Post Graduate Diploma
Degree : PGD
Mode : Correspondence
Medium : Distance Learning
Level : PG

Bioinformatics Bioinformatics - Future of Biological Research 21st century is considered to be information technology era that has created an immense impact in every sphere of life leading to knowledge transfer i.e. outsourcing of information. Information is Knowledge and Today’s economy is Knowledge economy . Bioinformatics is a interdisciplinary subject between biological information and IT. Recent developments of the sciences have produced a wealth of experimental data of sequences and three-dimensional structures of biological macromolecules. With the advances of computer and information science, these data are available to the public from a variety of databases on the Internet. Bioinformatics has been defined as the science of examining the structure and function of genes and proteins through the use of computational analysis, statistics, and pattern recognition. A number of recent workforce studies have shown that there is a high current and unmet demand for people trained to various levels of expertise in bioinformatics, from technicians and technical librarians to developers of new and improved methodologies and applications. Bioinformatics is a rapidly evolving and developing field both in terms of breadth of scope of useful applications and in terms of depth of what can be accomplished. National estimates of needed positions in the field in the next four to five years are about 20,000. Bioinformatics: Key to Science and Technology's Future Evaluation &Certification - Assignment Based For more details like career prospects visit www.ibri.org.in

One Week Short Term Courses
View Program Details
Category :
Degree :

Life Sciences, Biotech, Bioinformatics, Clinical Trials & Information Technology IBRI has introduced One Week Workshops for students to utilize their summer vacations in order to gear /train themselves for 21 st Century Knowledge-Led-Economy. The Workshops are on the topics/domains which will Increase Excellence for Breakthrough in Career Competency Earning Value. S.No Workshop On Duration Eligibility 1 Genomics & Proteomics One Week Graduate/PG/Professional 2 Next Generation Sequencing One Week Graduate/PG/Professional 3 Computer Aided Drug Designing & Cheminformatics One Week Graduate/PG/Professional 4 Human Genetics; Concepts, Methodology & Applications One Week Graduate/PG/Professional 5 Clinical Trials One Week Graduate/PG/Professional 6 Biostatistics & Research Methodology One Week Graduate/PG/Professional 7 Database Management Systems & Biological Database One Week Graduate/PG/Professional Computer Sciences Workshops One Week Graduate/PG/Professional 1 Information Technology: Basics One Week Graduate/PG/Professional 2 Database Management Systems One Week Graduate/PG/Professional 3 E- Commerce One Week Graduate/PG/Professional 4 C,C++, asp.net, Php, and more One Week Graduate/PG/Professional For more details like career prospects visit www.ibri.org.in

Certificate Course in Molecular and Human Genetics
View Program Details
Category : Other Medicine Certificate Courses
Degree : Certificate
Mode : Full Time
Medium : Campus
Level : Certification

certificate course in Pharmacovigilance
View Program Details
Category : Other Medicine Certificate Courses
Degree : Certificate
Mode : Full Time
Medium : Campus
Level : Certification

Master in Bioinformatics
View Program Details
Category : Bioinformatics
Degree : M.Tech.
Mode : Full Time
Medium : Campus
Level : PG

M.Tech. Bioinformatics - Stands for Master of Technology in Bioinformatics. Typically, a M.Tech is a two year degree, minimum eligibility for which is a B.Tech. in Bioinformatics. Bio-Informatics is essentially the application of computer science and information technology to the field of molecular biology.

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Name : Indian Biosciences and Research Institute
Location : C-50, First Floor, Sector-2
City : Noida
State : Uttar Pradesh
Country : India
Contact No : +91-9999 509892
Contact Email : info@ibri.org.in
Website : www.ibri.org.in   
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