Service: Pharmacovigilance (human medicines)

• New CTIS Safety Module for Annual Safety Reports goes live on 28 September 2026

  09.09.2026

  

• Additional risk minimisation measures (aRMMs) – from requirement to implementation

  24.07.2026

  

• Embedded expert support for RA & PV teams: a flexible alternative to hiring and full outsourcing

  13.05.2026

  

• Global healthcare company & Medfiles: ensuring quality and continuity in post-approval RA and PV activities

  04.05.2026

  

• How do post-marketing drug safety practices differ between Japan, the US, and the EU

  07.04.2026

  

• What are the MAH’s post-authorisation pharmacovigilance responsibilities

  10.03.2026

  

• Major pharmacovigilance reform: EU Regulation 2025/1466 sets new standards for MAHs

  12.02.2026

  

• Looking for a reliable medical information service provider?

  16.01.2026

  

• Medfiles and LINK Medical: partners in regulatory and pharmacovigilance services in Northern Europe

  28.05.2025