We translate a wide variety of documents to support every stage of the clinical research and drug registration process, including pre- and post-marketing documentation.

Our most common translation projects include:

  • Informed consent forms (ICFs) and informed assent forms
  • Clinical trial agreements
  • Clinical trial protocols and protocol synopses
  • Patient information sheets
  • Patient diaries
  • Patient questionnaires
  • Emergency cards and patient cards
  • Regulatory documentation and approval
  • Correspondence with ethics committees and regulatory authorities
  • Ethics committee opinions
  • Clinical study results, case studies, and scientific publications
  • Summaries of product characteristics
  • Package leaflets
  • Medicinal product labels

other specialisations