This course provides a practical, end-to-end overview of the clinical study startup process. It covers study feasibility and site selection, pre-study site visits, site initiation, informed consent, and subject recruitment and retention.

Learners will gain hands-on understanding of essential documents, Trial Master File (TMF), and site readiness activities. The course also explains regulatory, ethical, and operational requirements that govern study activation.

By the end, participants will be equipped to efficiently initiate, document, and operationalize clinical trials in compliance with global regulations.

Indian students: Choose the Offline Payment option at Checkout. Once your Order is created you will receive an email with a link to complete your payment of INR 19,999.