Consumer Health
ClinChoice has the skills and experience to prepare high-quality reports that are critical in receiving regulatory approvals. Whether done as part of a clinical trial or as a stand-alone project, our medical writers at ClinChoice combine medicine, science, and technical writing to deliver precise documents intended for the target regulatory submission.
Medical Writing Services
ClinChoice conducts literature research for authoring reports and has undertaken a wide range of medical writing assignments.
- Protocols
- Clinical study reports
- Technical document
- Case narratives
- Abstracts and manuscripts
- Documentation for Congress exhibits
- Investigator’s Brochures (IBs)
- Orphan Drug Dossiers
- Investigational Medicinal Product Dossiers (IMPDs)
- Investigational New Drug (IND) documents
- Pediatric Investigation Plans (PIPs)
- Risk Management Plans (RMPs)
- Common Technical Document (CTD/eCTD)