The quality of written clinical presentations can play a critical role in the success or failure of new compounds and devices.

InnoPharma’s medical writing service is qualified to help you in compiling, organizing, writing, editing and producing a wide range of medical or scientific documentation required to support your product development efforts: Clinical Development Plans, Protocols, Clinical Study Reports (Phase I – IV, clinical and non-clinical sections of the CTD, i.e., Clinical Overview, Clinical Summary, Non-Clinical Overview and Non-Clinical Summary, Investigator Brochure, Informed Consent, Periodic safety update reports (PSURs) and other pharmacovigilance documents, Preclinical study reports, expert reports and summaries as well as abstracts, manuscripts, and journal articles are only a sample of the products that InnoPharma’s medical writing team can offer you.