Clinical Research and Post Approval Services

Clinical Writing

Providing documentation from initiation to end of the study

Sciformix has a team of experienced writers who can deliver Protocols, Informed Consent Documents as well as Clinical Study Reports to support clinical studies across all phases of product development, including, non-interventional and outcomes research studies. The writers work in close collaboration with cross-functional teams, including clinicians, medical reviewers and biostatisticians, and have a sound understanding of the drug development process and ability to understand and analyze scientific data.

We have broad-based expertise in several therapeutic areas, and types of documents include, but are not limited to the following:

  • Protocols
  • Informed Consent Documents
  • Clinical Study Reports
  • Subject Narratives
  • PHRMA Web Synopses
  • Module 2 Summaries of Efficacy and Safety (ISE & ISS)

Read more about our Clinical Writing services by completing the brief form below.

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