Masterclass Regulatory Approval (MDR / FDA)

Van derden

05/11/26

Are you a Dutch Life Sciences & Health (LSH) company looking to bring your medical technology to international markets?

Regulatory approval is a critical step in international growth, but navigating an increasingly complex regulatory landscape can be challenging. From evolving European requirements under the Medical Device Regulation (MDR) and In Vitro Diagnostic Regulation (IVDR) to FDA requirements in the United States and additional country-specific regulations, regulatory pathways can have a significant impact on international market access.

During this Health Holland Masterclass, Task Force Health Care and MedEnvoy Global will bring together regulatory expertise and practical experiences to explore the latest developments, challenges and considerations for Dutch LSH companies navigating international regulatory approval.

Join us to strengthen your regulatory knowledge and prepare your organisation for international growth.