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:
- 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.