Distance Learning

Post Gradudate Diploma in Monitoring of Clinical Trials

✔ ACCRE USA Accredited
✔ Program developed by senior industry experts
✔ eBooks – Presentation & Notes on Cliniminds LMS
✔ Cliniminds Certification after completion of program
✔ MCQ based final exams
✔ Introduction to Clinical Research & Phases of Clinical Trials | Indian Schedule Y & Other Guidelines | Ethical Considerations in Clinical Trials | Sponsor/Vendor Responsibilities | Essential Documents in Clinical Research | Protocol Writing | CRF Design | Site Selection Process | Pre-study Site Visits Monitoring | Site Initiation Monitoring | Routine Monitoring Visit | Case Report Form Review and Source Document Verification | Safety Reporting Monitoring | Study Drug Accountability Monitoring | Site Close-out Monitoring | Investigator Responsibilities | Informed Consent – Process & Documentation | Investigational Site Audits