Development and registration of new medicines is complex and involves many documents and strict deadlines. We ensure timely delivery and consistent quality. Our outstanding teams of medical and pharmaceutical translators draw on years of experience and are wholly familiar with the requirements imposed by both national and European medical regulatory authorities.
You can have complete confidence that translations will comply with the latest QRD templates, MedDRA terminology and EDQM Standard terms.
We are proud to support CBG-MEB and the EMA (European Medicines Agency).

We translate all documents that play a role during research and development, registration and use of medicines, including:

  • Summary of Product Characteristics (SmPC)
  • Packaging texts
  • Patient Information Leaflets (PIL)
  • Marketing authorization
  • Market introduction texts
  • Pharmacovigilance 

Contact us & tell us about your project.