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