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