Launching a new product? Scaling multilingual trials? Updating safety documentation for regulators? We help you move quickly and compliantly—without cutting corners.
We translate:
• Clinical trial documentation (protocols, ICFs, CRFs, SAPs, IBs)
• Pharmacovigilance reports (SAEs, SUSARs, DSURs, PSURs)
• Regulatory submissions (EMA, FDA, PMDA, MHRA)
• Labelling and IFUs for medical devices (UDI, MDR, IVDR)
• SmPCs, PILs, and PROs
• Public health campaigns and multilingual patient comms
• Adverse event reports and post-marketing updates
• Hospital SOPs and training modules
• eHealth content, mobile app interfaces, telemedicine platforms