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Clinical Research

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Clinical Research (Regular/Online)

Course Overview

Clinical trials are systematic investigations in human subjects intended to gather safety and efficacy data of a new drug. The clinical trials conducted all over the world follow universally accepted guidelines and regulations. These trials for new drugs are conducted on human subjects or patients only after abundant satisfactory information has been collected on its quality and safety through pre-clinical or animal studies and which have an approval from the required health and ethical authorities.

The Clinical Trials, Regulations, and Data Management Certification course offers a comprehensive, specialized and industry level executive and detailed curriculum covering clinical trial planning, ethics, ICH guidelines, and FDA regulations. The course focuses on data management, medical writing, and regulatory compliance, providing certification for professionals. Gain expertise in clinical trial design, randomization, and statistical analysis. Ideal for professionals in the pharmaceutical and healthcare industry, this course ensures up-to-date knowledge for clinical research, data validation, and medical documentation.

With a reputation for high-quality, cost-effective global clinical trials, Asia are fast becoming the hub for global clinical research. As the clinical trials market continues to expand, the lack of trained professionals and gaps in skill advancement need to be addressed to utilize the huge clinical research potential in the region IBRI has introduced the courses in Clinical Trials with an aim to bridge this 'Knowledge divide'. IBRI mission is to strengthen the clinical research capabilities in Asia by providing effective and cutting-edge educational and training programs in various aspects of clinical research. The institute fosters interactions with experts from industry, government and academic institutes to provide guidance in the development and implementation of training programs.


‘Key of success in life is to become a skilled first’



Post Graduate Diploma in Clinical Research

Course Paper Content
Paper:I Clinical Trials, ICH, Ethics, IRB and Regulations for Clinical Trials
Paper:II Clinical Trials Data Management, Computerized Systems for E- Case Report Form and Data Acquisition and Validation
Paper:III Biostatistics, SAS and Data Management
Paper:IV Basics of Good Medical Writing
Paper:V Practical and Project

Eligibility:

Candidates with MBBS / B.D.S / B.A.M.S / B.H.M.S /B. Pharmacy / BVSC/ B.Sc. (Nursing)/ M.Pharma/ Science Graduate/ Lifesciences Graduate/ DMLT/BMLT/Pharm D ..etc are eligible. Educational qualification and experience in the field of medical sciences, life sciences, data management, and clinical research. Even B,Sc(M.Sc) life sciences or B.Tech (M.Tech, B.Tech+M.Tech Dual) in Biotech are eligible for the course.

Fees:

Course Fees: Rs.35,000/- Only(One time payment)
 (Fees can also be paid in two installments i.e. Rs.20K and 15K.

Examination Fees:Rs.1000 only.

Course Fees: USD850 Only(One time payment)
 (Fees can also be paid in two installments i.e. USD550 and USD300

Examination Fees: USD100.
Note:
1-Exam fees are excluded from Course fees.

2-Payment is to be made through Cash / Demand Draft / At Par Cheque in favor of "IBRI-Unit of Exordior Technical Services Pvt Ltd." payable at "Noida/New Delhi".