| Eligibility - Lifescience Graduates & Postgraduates,B.Pharm, M.Pharm, B.P.T, M.B.B.S, B.D.S, B.H.M.S, B.A.M.S | ||
Duration: |
12 months | |
Type: |
Full Time (Total 600 Teaching Hours including 300 hours of theory, 200 hours of practical training and 100 hours of live industry project) |
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Fees: |
Rs. 1,85,000/- | |
Live Industry Project: |
Yes | |
Objective: |
The Post Graduate Diploma in Clinical Research Course (PGDCR) will provide quality inputs and an in-depth understanding of the important aspects of the clinical research process and prepare the students for entry level position in Clinical Research industry. It covers important aspects of drug development process, medical terminology, Basics of pharmacy, fundamentals of clinical research, clinical pharmacology and therapeutics, epidemiologic principles necessary for designing clinical research studies, Regulatory guidelines and ethics in clinical research, biostatistics, documentation, clinical trial management, Safety monitoring, financial aspects of clinical research, regulatory inspection and basics of medical writing. |
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| Eligibility - Lifescience Graduates & Postgraduates,B.Pharm, M.Pharm, B.P.T, M.B.B.S, B.D.S, B.H.M.S, B.A.M.S (candidates with prior work experience preferred) | ||
Duration: |
12 months | |
Type: |
Part Time (Total 250 Teaching Hours including 150 hours of theory, 100 hours of practical training) |
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Fees: |
Rs. 1,00,000/- | |
Live Industry Project: |
No | |
Objective: |
This course will provide knowledge and understanding of the various aspects of clinical research. It covers fundamental of Clinical research, Regulatory aspects and ethical principles involved in conducting clinical trial, biostatistics and research methodology, Clinical trial management, safety monitoring and reporting and basics of Medical Writing. |
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| Eligibility - B.Pharm, M.Pharm, M.B.B.S, B.D.S, B.H.M.S, B.A.M.S, B.P.T, M.Sc.Lifesciences | ||
Duration: |
6 months | |
Type: |
Part Time | |
Fees: |
Rs. 75,000/- | |
Objective: |
This course is designed for individuals who write or review documentation in relevance with Clinical trials and regulatory submissions. Upon completion of the course the individual will be able to have an understanding of what Medical writing encompasses, how to write documents as per the regulatory requirements, write an abstract, manuscript, therapeutic product leaflet. The course will also highlight presentation of Clinical data in an effective and scientific manner. |
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