We are 3 united scientific writers with more than 15 years of experience in the pharmaceutical industry. Our writing services span the entire product lifecycle, i.e. from regulatory writing to market access-related documents up to medical communications and medical education, for drugs and medical devices. Our services include, but are not limited to: - Regulatory medical writing: clinical study reports, clinical study protocols, Investigator's Brochures, informed consent forms, briefing documents, medical narratives, ... - Medical communications: slide kits, product monographs, global value dossiers, brochures, manuals, leaflets, detail aids, leave behinds, medical education materials, ... - Market-access related documents: we write up, layout and structure reimbursement dossiers to be submitted to the Belgian and Dutch Authorities, and prepare and submit additional RMA materials conform Belgian guidelines. - Medical publication: development of scientific manuscripts (for publication), abstracts and conference posters - Meeting and conference reports: we attend conferences, meetings and advisory boards and prepare reports/abstract/summaries/minutes that summarize and synthesize the main ideas, conclusions and recommendations of the key speakers. - Peer review & quality control: we perform a systematic and independent examination of clinical documents and materials for scientific accuracy, grammatical and editorial errors through an unbiased, independent critical assessment. - Layout & design: we design and improve the format of (medical) documents in different file types (.docx, .ppt, .xlsx, .pdf…) to an aesthetically pleasing and easy-to-read arrangement. - Medical translation: we translate (medical) documents from Dutch to English, Dutch to French, French to English and vice versa. Contact us at: info@chemistri.be or 0032/484.61.27.65 www.chemistri.be