Program Highlights

	A two-day training program aimed at providing basic to advanced level understanding on Clinical Research, Drug Development Process & Good Clinical Practice Guidelines.
	Focus Area: - Overview of Drug Development Process - Clinical Trial Processes - ICH-GCP Guidelines - Informed Consent Documentation - Pharmacovigilance - Essential Clinical Trial Documents - GCP Workshop - Clinical Trial Monitoring - Audits & Quality Assurance - Data Management - Drug Regulatory Affairs - Team Exercises etc.
	On completion a certificate is awarded by Catalyst Clinical Services Pvt. Ltd.

Target Audience: Clinical Research & Allied Professionals employed in Pharmaceutical Companies, CROs, Site Management Organizations, Research & Academic Institutions etc. 

Enrolment Type: Group enrolment (for a minimum of 10 participants)

Program Fee: Rs. 6000/- (Rupees Six Thousand Only) per participant excluding the travel/stay cost of the trainer.

For more details mail at info@catalystclinicalservices.com