Our outstanding teams of medical and pharmaceutical translators can draw on many years of experience and are wholly familiar with the requirements imposed by both national and European medical regulatory authorities.
You can be sure that the translation will comply with the latest QRD templates, MedDRA terminology and EDQM Standard terms.
Our valued relationship with the health authorities in The Netherlands (CBG-MEB) and the European Medicines Agency (EMA), along with their move to nearby Amsterdam, means that we are well positioned to make sure your projects run smoothly.

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.