Tag

Pharmaceutical advertising

Rules on advertising and information for medicines in Belgium, covered in MPCA's regulatory watch.

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.

Request a free consultation Our services

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
Services
Applications
Company
Contact

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

QP GMP RP GDP RIP EU QPPV/LCP