Medical Writing

We can support you with:

Outsourcing of specialists:

  • Medical writer

Ad-hoc support:

  • Clinical Study Protocol (CSP) or Clinical Investigation Plan (CIP
  • Investigator’s Brochure (IB)
  • Patient Information and Informed Consent Form (ICF)
  • Clinical Evaluation
  • Clinical Study Report (CSR) or Clinical Investigation Report (CIR)
  • Clinical Overview and Summary
  • Literature search
  • Non-interventional Study Protocol
  • Protocol for Post-marketing Safety and/or Efficacy Study
  • Post-marketing Clinical Follow-up (PMCF) Plan
  • Update of your Clinical Evaluation
  • Posters and Scientific Article

Beatrice Öström
Nordic Head of Scientific Affairs
Please contact:
Email
+46 70 165 22 38