Prime your clinical studies for worldwide success
Recruit study subjects
When your target patient population is international, you need to speak their language. Our clients have recruited study subjects in dozens of languages with translations for clinical trial authorizations and patient consent.
When your site has identified an adverse event or an adverse reaction, you have to act fast. Our teams are ready to translate SAE and SAR data and responses immediately so you can:
- ensure the safety of your trial subjects
- meet the reporting requirements of your EC and regulators
- monitor postmarket safety of your device or drug
- meet surveillance and pharmacovigilance requirements.
Submit for market approval
International regulatory bodies want to review your MAA requests in their own language. We translate your submission packages, including clinical data and final labeling, for your target markets.
So you can get on with improving lives.