DUBLIN--(BUSINESS WIRE)--The "Combination Products" conference has been added to ResearchAndMarkets.com's offering.
Combination products are especially challenging to register and maintain since they consist of two or more regulated components covered by different and usually independent sets of regulations in both the EU and US and various other regions.
Delegates working in this area must keep abreast of current and new legislation in this complex area to ensure a good regulatory strategy and compliance of their products.
This seminar provides Professionals working in this area with:
- A thorough understanding of the complexities involved
- All the relevant regulations and guidelines
- Real life examples of how to register and maintain various types of combination products
- Interfaces: Change Management and LCM
- Compliant safety reporting for combination products
- Documentation requirements and interfacing
Areas Covered in the Session:
- Documentation requirements and interfacing
- Documentation requirements for combination products EU
- Documentation requirements for combination products US
- Interfacing, development, quality, regulatory
- Managing third parties and document control
Who Should Attend:
- Clinical Trial Managers
- Medical Officers
- Regulatory Affairs
For more information about this conference visit https://www.researchandmarkets.com/research/55q5zz/two_day_pharma?w=4
