Translation & Revision
InfarAMA translates and/or revises all documents related to marketing authorization applications and also to post-marketing period/phase for medicinal products such as .. SPCs, leaflets, labels, RMA, Expert reports, Inspection reports, Scientific articles, Letters from Health Authorities, documents related to pharmacovigilance, documents related to publicity and training material.
Our translations are compliant with the latest QRD templates, MedDRA terminology and EDQM Standard terms.
InfarAMA also translates and revises documents related to medical devices and food supplements.
InfarAMA generally offers translations from and into the following languages: EN, FR, DE, NL. However, do not hesitate to contact us if you need a different language combination.