Clinical Regulatory - Pack of 11 Webinars

This exclusive Pack of webinars contain 11 courses: 

1. Good Clinical Practices Review of ICH E6 (R3) Latest Guidance 

2. Trial Master File Requirements and Essential Regulatory Documents 

3. Selecting and Managing Vendors in Clinical Research 

4. Risk Management in Clinical Research 

5. FDA’s GMP Expectations for Phase I and First-In-Man Clinical Trials 

6. GCP Compliance - Audit Preparation and Inspection Readiness 

7. How to Best Document Clinical Evaluation Report (CER) for CE Mark 

8. Clinical Project Management 

9. Successful FDA Meeting Preparation and Conduct 

10. Medical Device Clinical Investigations to the new EU MDR Requirements 

11. EU's New Regulation 535/2014 on Clinical Trials - Insights into Effective Clinical Trials