We handle the registration of your medical products
The issue of registering medical products is an important and time-consuming one for the medical technology industry that we would like to complete on your behalf.
Bringing a medical product to market requires comprehensive checks and tasks, such as implementing a conformity assessment procedure, in order to receive the registration.
Take advantage of our experience! No matter the country of use, we can prepare your medical products for the international requirements as well as coordinate and implement registration including for the
- European market
- American market
- Canadian market
- Chinese market
- Japanese market
- Other markets on request
We can offer the following support for registering your medical products:
- Strategic advice and project management for product registration
- Communication with public authorities and designated organisations
- Researching the relevant requirements, rules, norms, standards, guidance
- Advice on regulatory issues when developing new products
- Classification of medical products including their purpose and indications
- Producing the necessary registration documentation and carrying out the registration
