ClinChoice has the skills and experience in preparing 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 expert medical writers combine medicine, science, and technical writing to deliver precise documents intended for the target regulatory submission.
Pharma & Biotech
Medical Writing Services
ClinChoice offers a wide range of services throughout your product’s lifecycle.
- Clinical Study Protocol Development
- Investigational Medicinal Product Dossiers (IMPDs)
- Informed Consent Documents
- Patient Diary/Patient Educational Materials
- Clinical study reports
- Pre-IND and IND Submissions
- Regulatory Marketing Authorization Application/BLA/NDA
- Gap Analysis of available clinical modules
- Independent QC of all regulatory medical documents
- Medical Communication (Manuscripts/Publications/Case Studies/Posters)
- DSUR