Product: Human medicines

• Outsourcing local regulatory affairs: 4 examples of tailored support in the Nordics and Baltics

  08.10.2026

  

• From study planning to reporting – 20 years of experience in clinical research and scientific writing

  06.10.2026

  

• Medfiles contributes to advancing clinical research in Finland through FINCRO

  14.09.2026

  

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

  09.09.2026

  

• Selected non-prescription medicines to be sold outside pharmacies in Finland

  08.09.2026

  

• Cooperating with Baltic medicines authorities in regulatory submissions: Practical experiences from Estonia, Latvia and Lithuania

  25.08.2026

  

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

  24.07.2026

  

• Flexible regulatory outsourcing: choosing the level of support that fits your needs

  22.07.2026

  

• How to obtain a marketing authorisation in the EU – requirements and approval process for medicinal products

  26.06.2026