Content
Successful market entry in Europe is usually followed by the desire to enter markets outside the EU. In order to design this successfully, it makes sense to know some basic requirements and procedures. The IMDRF concepts are particularly helpful here, but early internal precautions also help to successfully approve the products. The seminar creates the basis for the preparation and submission of approvals worldwide.
Topic overview
- Basic requirements for approvals
- Interesting concepts from WHO and IMDRF
- Relevant precautions for successful market entry
- Re-registrations, QM certifications and associated documentation
target group
Employees from the areas of regulatory affairs and quality management, those responsible for placing on the market, employees responsible for compliance with national and international legal regulations.
Prior knowledge
Basic knowledge of marketing in Europe and DIN EN ISO 13485 is recommended.
Funding opportunity
ESF funding is possible. Further information can be viewed here .
Early bird discount
If you register up to 3 weeks before the start of the seminar, you will receive an early bird discount of 10 percent.
KONTAKT:
Online
