Tag

Regulatory compliance

Practical regulatory compliance for the life-sciences sector in the Benelux, from MPCA's regulatory watch.

MPCA International - EUDAMED mandatory from 28 May 2026 Medical Devices
11 jun 2026

EUDAMED becomes mandatory from 28 May 2026: what to do now

From 28 May 2026 the first four EUDAMED modules become mandatory under MDR and IVDR. Here is what...

Read more
MPCA International - Article 10 and the Responsible Person for Information and Publicity (RIP) in Belgium Regulatory Affairs
11 jun 2026

Article 10 and the RIP role: takeaways from the FAMHP info session

Several MPCA colleagues attended the FAMHP’s info session on Article 10. Here is what the updated guidance means...

Read more

Need help navigating the Benelux regulatory landscape?

Our team of specialists is ready to support you — from regulatory strategy and pharmacovigilance to market access and quality assurance.

Your reference partner for Regulatory Affairs, Pharmacovigilance and Quality Affairs in the Benelux. Active since 1998 from Ghent, Belgium.

Accreditations

QP GMP RP GDP RIP EU QPPV/LCP

© 2026 M.P.C.A. International BV  ·  Privacy policy  |  Cookie policy

QP GMP RP GDP RIP EU QPPV/LCP