The Clinical Trials Information System (CTIS) is used for submitting clinical trial applications to the European Medicines Agency (EMA).
If you need support with your clinical trial application, we can help.
Or are you still planning your clinical trial design?
Our team of experts can also help you design your clinical trial and put together the essential documentation such as the study protocol, subject information and informed consent, etc.
Contact us so we can discuss your specific needs.
