Product: Human medicines

• Global pharma company & Medfiles: cooperation in obtaining and maintaining marketing authorisations in the EU

  08.03.2024

  

• Six reasons to engage regulatory CMC experts in drug development at an early stage

  20.02.2024

  

• Marketing authorisation application processes efficiently under one roof – for all EU countries

  12.02.2024

  

• Free Guide: What you need to know about active substance registration strategy?

  12.01.2024

  

• Herantis & Medfiles: 15 years of collaboration in clinical trials

  27.11.2023

  

• The annual Lääketurvaseminaari event offers a broad overview of current topics and future trends in pharmacovigilance

  06.07.2023

  

• Longer lifecycles call for better quality – changing your eCTD publisher might be the solution

  05.06.2023

  

• CRA ensuring success of clinical trials

  19.05.2023

  

• Free guide: Determining storage conditions for pharmaceuticals

  10.05.2023