Diploma in Clinical Research

This is a foundation educational program, designed for all the candidates aspiring to work in the field of clinical research or allied professions like central labs. The program provides complete overview and practical environment in the field of clinical research. The program would allow candidates to upgrade their knowledge about ICH GCP Guidelines, regulatory issues and other major aspects of clinical trials management. Select important topics from the following groups would be covered in the program:
- Clinical Research Introduction
- Roles & Responsibilities of Key Stakeholders
- Preparations & Planning for Clinical Trials
- Essential Documentation in Clinical Research & Regulatory Submissions
- Clinical Trials Project Planning & Management
- Study Start Up Process
- Clinical Monitoring Essentials
- Compliance, Auditing & Quality Control in Clinical Research