Service: Medical device and IVD clinical evaluations and investigations

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

  06.10.2026

  

• Why early regulatory involvement accelerates medical device and IVD innovation

  16.09.2026

  

• Medfiles contributes to advancing clinical research in Finland through FINCRO

  14.09.2026

  

• ISO 14155:2026 – What’s new for medical device clinical investigations

  20.07.2026

  

• How to document and keep IVD performance evaluations up to date under EU IVDR

  06.07.2026

  

• When and how to conduct IVD performance studies under EU IVDR

  18.05.2026

  

• How to gather clinical evidence for IVD performance evaluation under EU IVDR

  12.03.2026

  

• Q&A: EU MDR and IVDR notified body processes and transition periods explained

  07.01.2026

  

• When does your medical device need a clinical investigation?

  14.11.2025