Trial Management
The center offers a range of services to support investigators, institutions and pharmaceuticals in aspects of trial set-up, trial conduct, and trial close-out with a focus on the health and protection of research participants. Our center’s experienced trial management teams ensure that the study objectives and timelines are met. Our trial management services include:
- Regulatory Submission
- Contracts Management
- Assistance with site selection
- Site initiation visits
- Monitoring services
- Report preparation
- Ethics applications
- Trial master file management
- Standard operating procedures preparation
- Study specific manuals preparation
- Participant information sheet and informed consent form preparation
- Training of site investigators and staff