Medical writing is an indispensible part of clinical research. Our highly experienced medical writers know this, delivering each component document as an integral part of a much wider clinical regulatory documentary process. Wherever possible, we involve our writers in the study design so that when the data is ready for reporting, they are already familiar with the required output format.
Synergy’s professional writing team has experience working for a diverse range of customers, covering over twenty therapeutic areas, including oncology, cardiovascular, anti-infectives, respiratory, pain, virology, devices and metabolic diseases. We work with clients ranging from academic groups and virtual clients to global pharmaceutical and spin-out biotechnology companies.
We are experts in authoring the full range of clinical regulatory documents, in particular:
ICH GCP compliant clinical study protocols
Investigator protocol and brochures
Clinical study reports
Patient narratives
Clinical sections of the Common Technical Document (CTD)
We also provide a wider scope of writing services, including authoring literature reports, manuscripts and Standard Operating Procedures (SOPs) or working procedures, as well as a document quality control service.
All of our work is reviewed, edited and delivered to the highest ethical and scientific standards.