CURRENT ETHICAL & REGULATORY REQUIREMENTS FOR CLINICAL TRIALS/RESEARCH

AN AWARENESS PROGRAM

WHEN

May 10, 2016, 9am-6pm

WHERE

ANIIMS, Port Blair

Objective:

To strengthen and empower the IEC members, clinicians and investigators to ensure that they understand scientific, regulatory norms, ethical design, conduct and reporting of clinical research that will be of uniform nature and meets national and international quality standards.

CONDUCTED BY:

CLINICAL DEVELOPMENT SERVICES AGENCY (CDSA) ( An extramural unit of THSTI), Dept. of Biotechnology, Ministry of Science & Technology,Government of India

LOCAL ORGANISING SECRETARY

DR. C. DINESH M. NAIDU
Professor & Head of Pharmacology,
ANIIMS, Port Blair.
Email: drcdineshnaidu@gmail.com
Mobile: 7063929151

No Registration Fee

WHO CAN ATTEND

Members from Ethics Committees, Clinicians, Investigators, Clinical research team members.

OUTCOMES

Create an awareness about current guidelines & regulations for the conduct of clinical research in India so as to ensure that the trial subject's right, safety and well-being are well protected.

BENEFITTING


• Ethics Committee Members
• Clinical Investigators

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