Our medical writing solutions are designed to support your clinical trial, regulatory, and publication writing needs.
We deliver high quality documents in a timely manner, while offering our clients the flexibility to choose between our full-package writing service and single-document writing and revision.
From Clinical development to post-marketing studies...
We support our clients starting with study design in collaboration with key experts in different therapeutic areas, through the whole study, offering Clinical Study Protocol, Informed Consent Forms, Clinical Study Report, and Patient Narratives writing services.
Our services include the preparation and update of Regulatory Documents such as Investigator Brochure (IB), Common Technical Document (CTD), and Investigational Medicinal Product Dossier (IMPD).
We support our clients in different publication types, handling the whole process of writing publications and scientific journal submissions, while handling revisions and responding to reviewers/editors.
Our services also include Advisory Board Meeting minutes reporting and Medical Translation Services for different material
2019: Our clients include 8 of the 10 top pharmaceutical companies worldwide.