From regulatory documents to scientific communication.
01 · Regulatory affairs
Pharmaceutical product dossiers and certificates, package inserts, packaging materials and stability studies.
02 · Clinical research
Protocols, informed consent forms and investigator's brochures. CIOMS reports, case reports, patient diaries, ethics committee letters and amendments.
03 · Medical and scientific content
Scientific articles and publications, specialist interviews, workshop materials and product promotional literature.
04 · Pharmaceutical technical documentation
Machinery manuals and technical documentation used in the pharmaceutical industry.
Scientific expertise.
Pharmaceutical oversight.
Our team brings together specialized translators and professionals with backgrounds in pharmacy, medicine, chemistry and health sciences.
DMV provides pharmaceutical technical oversight of specialized content in this field.
We understand the conceptual and terminological precision required in regulatory and clinical documentation.
From a single document to large volumes.
We tailor each proposal to the specialty, scope and project schedule.
When contacting us, please specify the document types, source and target languages, and target date. This enables us to confirm the scope, schedule and quotation.