Medical writing is a speciality that requires professionalism as well as an in-depth understanding of French protocol requirements and regulations. Presenting a well-crafted, targeted report that supports the desired outcome is integral to the process. Companies that intend to enter the French pharmaceutical market need to adhere to standards for medical writing and requirements for the publications of clinical trial results. Services include trial protocol (ICH), ICF, CRF and appendices, a clinical study report (ICH), scientific communication (abstract, poster, peer-reviews), regulatory drug dossier expertise (CTD) and quality assurance site inspection (GCP compliance). Contact BG Clinical Solutions via our contact form so we can provide you our expertise in clinical development.