target group
Managers and employees of Regulatory Affairs.
content
Canada, Brazil, Mexico (and more) are emerging as promising consumer markets. As in the EU, the authorities there require various documents for approval. In this seminar, the participants get to know similarities and differences to CE certification. You will also receive an overview of the documents to be submitted.
topic overview
- Regulatory requirements compared to Europe
- Quality management system requirements
- registration dossiers
- Competent authorities and representation in the country
- Procedure & case studies
previous knowledge
Knowledge of the EU MDR and DIN EN ISO 13485 is recommended.
KONTAKT:
Max-Planck-Straße 17, TuttlingenBeruflichen Bildungsstätte Tuttlingen & Online
