Pharma & Biotech

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.

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

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