In the countries of our operations certain documents should be translated into local languages for submission purposes, as well as for smooth study conduct. SynRG routinely translates or organizes translation of all required documentation:

• Study protocol
• Investigator brochure
• Informed consent forms
• Patient information sheets
• Patient’s diaries
• Investigator Product labels
• Case Report Forms
• Study manuals
• IVRS dialogues
• Investigator Site / Investigator agreement
• Regulatory and Ethics study approvals
• Correspondence with Competent Authorities / Ethics Committees
• Other study documents