International Product Registration: What documents are required? 2015 is an event dedicated to international product registration for IVDs & Medical Devices.
International Product Registration: What documents are required? 2015 covers topics such as:
- Role and responsibilities of US manufacturers & in-country distributors
- International regulation- Overview of country by country differences
- Working with in-country distributors
- Identifying the key players
- Types of documents need
- Sales forecasting – Who needs to know?
- Best practices for document legalizations
- Medical Device & IVDs
- How to get documents embassy legalized
- Apostille vs. Authentications
- Pitfalls – What to look out for
International Product Registration: What documents are required? 2015 brings together:
- Product Managers
- Regulatory Affairs Specialist/Managers
- Administrative Professionals working in Regulatory
- Marketing Professionals
