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Cooperation between inteQRA and Forcentis
We are looking forward to the partnership with Forcentis! Together with Forcentis, we can offer a comprehensive...
Regulatory requirements in medical technology are constantly evolving, particularly with regard to sustainability and new legal requirements for medical devices.
In addition, there are cross-industry developments such as the issue of PFAS, which is becoming increasingly important and also has a major impact on the medical technology industry.
We keep the overview for you: well-founded, up-to-date and practical. Thanks to our close networking - including as a member of Swiss MedTech - we are always up to date. This enables us to support you in developing safe and sustainable solutions.
Would you like to know what this means for your product?
Contact us - we will be happy to provide you with individual and expert advice.
