Content
Great Britain and Switzerland will continue to be important sales markets even after the markets have been decoupled. In the course of this, independent regulatory requirements will be established for these markets. In this seminar, participants will learn about the newly created regulatory structures. The registration and information obligations are also discussed. Furthermore, the current status of admission routes is presented.
Topic overview
- Regulatory requirements in the respective countries
- Approval routes for different products
- Competent authorities and representation in the country
- Necessary quality management systems
- Process and case studies
target group
Managing Director and Employee Regulatory Affairs.
Prior knowledge
Knowledge of the EU MDR and DIN EN ISO 13485 is recommended.
Notice
Participation in the seminar “Fundamentals of Regulatory Affairs International” is recommended in advance.
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:
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