Regulatory support and applications
UCR provides support for regulatory interactions and the preparation and management of applications for clinical studies.
This is how we can support you
- Ethics applications
Support in preparing application documents - Regulatory submissions
Preparation and submission of applications in line with current requirements - Documentation
Study protocols, patient information and supporting documents - Dialogue with authorities
Support with questions, communication and responses to requests - Study registration
Management of registrations in relevant systems, such as CTIS
Contact us
Need support with regulatory requirements or study applications? Get in touch to learn more.