Consulting
Regulatory advice for medical devices

You need a partner to support you to launch your products on the Swiss market?

If you are a medical device manufacturer outside Switzerland and need an overview of the regulatory requirements of the Swiss market, PrimaMed has developed efficient methods to support you in the best possible way.

Possible steps for your success:
1. non-binding initial consultation
2. gap analysis
4. optional appointment of a national representative
5. support in the preparation of the required documentation, labeling and quality management system
6. registration of market participants and products
7. continuous monitoring and optimization

The close and trustful cooperation with you is our self-evident basis for the adequate and successful introduction of your products on the Swiss market.