The professional medical writers at ClinChoice combine medicine, science, and technical writing to deliver concise documents for regulatory, project management, and final reports throughout post-marketing surveillance.
Pharma & Biotech
Post-Marketing Services
ClinChoice conducts literature research to author reports and meet post-marketing requirements in pharmaceuticals.
- PBRERs, PSURs, and PADERs
- RMP and REMS
- Canadian aggregate reports
- Addendum reports
- Addendum to clinical overview
- Ad-hoc BR evaluation reports
- Responses to the regulatory authorities