Clinical Research (CR) Course

Service Description

Following Topics will be cover during course :- Introduction to Clinical Research Industry and Basics of Clinical Trials Drug Development Process Ethics and Ethical Guidelines for Clinical Trials and Good Clinical Practice (GCP): ICH Good Clinical Practice E6 (R2) Indian GCP and Schedule Y Regulations Guiding the Clinical Research Industry- History and Basics of National and International Regulatory Bodies Essential Documents in Clinical Trials: Protocol, CRF, Inform Consent, Investigator's Brochure, Study Progress Report Clinical Trials -Latest updates : New Drugs and Clinical Trials Rules, 2019 Industry Based Case Studies