The Global Medical Device Regulation 2016 is a course dedicated to the global regulatory strategy for medical devices.
Topics
- Points to consider in the development of a global regulatory strategy
- Elements impacting the definition and classification of medical devices globally
- Sources of regulatory and competitive intelligence
- The tools for global regulatory strategy development
- Develop a regulatory plan by applying global regulatory principles
- Elements of a regulatory plan
Who should Attend
Attendees from Regulatory professionals working in the medical device field.
