Medical Writer

Full services supporting the clinical evaluation process and clinical evidence development to ensure successful regulatory file audits under MDD and MDR including:

  • clinical evaluation plans (CEP) and reports (CER)
  • post-market surveillance (PMS) plans and reports
  • post-market clinical follow-up (PMCF) plans and reports
  • summary of safety and performance (SSCP)
  • user surveys
  • clinical study reports
  • conference posters
  • manuscripts