Collaborate with us

CVCTU is a hub for Clinical Trials of Investigational Medicinal Products (CTIMPs), non-CTIMPs (encompassing trials of complex interventions), and device studies. Whether it's a single-centre study or a national or international initiative, we have the skills and experience necessary to support a variety of investigator-led projects. 

At the CVCTU, we're here to ensure your trials are not only well-executed but also contribute to the advancement of cardiovascular knowledge on both local and global scales.

What services will the Barts CTU provide?

We can provide the following services:

• Trial management:
• Design
• Risk assessments
• Protocol and essential document development
• Obtaining regulatory and ethical approvals (MHRA, HRA, REC, CAG)
• Study oversight
• Data Management
• Database build
• Data management
• Central monitoring
• CRF design
• Statistics
• Randomisation
• Statistical design
• Statistical analysis
• Independent statistics
• Pharmacovigilance/Safety reporting
• Emergency un-blinding
• IMP management

Working with us

To enquire about CVCTU support please complete our enquiry form. A member of the team will then be in touch to discuss your proposals and assist in the submission process. The Study will then be reviewed by the CVCTU Scientific & Resource Committees.

We recommend getting in touch at the point of grant application development as this will enable you to take full advantage of our experience and expertise. 

Contact

Barts CVCTU Cardiovascular Clinical Trials Unit (CVCTU)
William Harvey Research Centre
Barts and the London School of Medicine and Dentistry
Queen Mary University of London
Charterhouse Square
London, EC1M 6BQ

Email: CVCTU@qmul.ac.uk