Advanced Program in Clinical Research – APCR

(Part Time)

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
• Quality Audits Inspections & SOPs

Classroom teaching by eminent faculty involving Lectures and Power Point Presentations.
• Detailed Syllabus for each Topic will be provided along with the course material


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

For more details call on 08511188845 or email on

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