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Great Britain and Switzerland will remain 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, the participants get to know the newly created regulatory structures. In addition, the registration and information obligations are discussed. In addition, the current status of admission paths 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
- Procedure & case studies
target group
Managers and employees of Regulatory Affairs.
previous knowledge
Knowledge of the EU MDR and DIN EN ISO 13485 is recommended.
KONTAKT:
Max-Planck-Straße 17, TuttlingenBeruflichen Bildungsstätte Tuttlingen & Online
