Part Time – APCR

Advanced Program in Clinical Research – APCR

Course objective: It focuses on the essential principles of Clinical Research and standard regulatory controls necessary to study the safety and efficacy of a drug. The course content has been reviewed and approved by Clinical research experts and academicians where more emphasis is laid on Planning, conducting, monitoring and generating information as per global standards and regulatory requirements. Students are not only trained in Clinical Research but there is a special focus given to Management & Soft Skill learning.

Duration of the course: Comprehensive 6 months Part Time Program.

Course Timings and Schedule: 1.5 -2 hours classroom training, scheduled on Sundays.

Eligibility

M.B.B.S, M.D, M.S, D.N.B, D.M (Interns are also eligible)
B.D.S, M.D.S, B.P.T,
B.A.M.S, B.H.M.S, B.U.M.S
M.Pharm, Ph.D
Working Professionals

Course Content

Introduction to Clinical Research, Clinical Pharmacology & Drug Action
Regulatory Affairs
Bio availability & Bio equivalence studies
Ethics in clinical Research
Global drug Regulations
Clinical Trial Design
Pharmacovigilance
Clinical Data Management & Biostatistics
Project Management & Clinical Trial Documents

Note:

To avail certificate & placement services, required to meet course passing marks criteria

* “Fees (Registration & program fees) once paid will not be refundable”