MSc Modules
The course content has been designed to provide students with the knowledge, skills and practical experience they need for an enhanced career in regulatory affairs.
It is comprised of the following segments:
Modules
- Principles of European Medical Technology Regulatory Affairs (RA)
- Design, Development and Testing of Medical Technology
- Clinical Evaluation of Medical Technology
- Management of Regulatory Affairs and its Contribution to the Medical Product Lifecycle
- Medical Device Vigilance, Post-Market Surveillance (PMS) and Risk Management
- Regulation of Drug-Device Combinations and Other Medical Technology Products
- US Regulation of Medical Technology
- Regulatory Strategy in the Market Place
