Diploma in Clinical research & Clinical trials
About Course
This diploma offers in-depth training in the methodologies and regulations of clinical research and trials. It covers study design, ethics, regulatory compliance (ICH-GCP), protocol development, patient recruitment, data management, and safety reporting—equipping students for roles in CROs, hospitals, and pharmaceutical companies.
Course Content
Diploma in Clinical research & Clinical trials
-
Medical writing in clinical research
00:00 -
1 The Evolution of Clinical Research. From Ancient Trials to Modern GCP times
00:00 -
2 Understanding Clinical Trials. The Roles of CRAs and CRCs Explained
00:00 -
3 Understanding the Role of Ethics Committees in Clinical Trials
00:00 -
4 Exploring the Key Stakeholders in Clinical Research. Roles and Responsibilitie
00:00 -
5 Essential Documents in Clinical Trials. A Comprehensive Guide
00:00 -
6 The Crucial Role of Regulatory Authorities in Healthcare
00:00 -
The Essentials of Clinical Trial Monitoring and Design
00:00 -
Exploring Clinical Trials. From Pharmacovigilance to Precision Medicine
00:00 -
The Importance of Clinical and Academic Research
00:00 -
Exploring the Role of Regulatory Authorities in Clinical Research
-
Understanding Clinical Trials. A Guide to Key Terms
00:00 -
Understanding Clinical Trials. A guide to key terms 2
00:00 -
Understanding Clinical Trials. A guide to key terms 3
00:00 -
Critical appraisal of research paper publication
00:00 -
How to write an academic article and academic writing
00:00 -
Research data management
00:00 -
Hazard and risk at work
00:00 -
Self reflection healthcare professionals
00:00 -
Leadership
00:00 -
Healthcare management podcast
00:00 -
Clinical trial protocols and management
00:00 -
Cardiology clinical trials part 1
00:00 -
Cardiology clinical trials 2
00:00 -
Cardiology clinical trials 3
00:00
