
Our Capacities
We identify the key sites and investigators to ensure your protocol is prioritized and implemented with primary outcomes and patients safety as the priority.
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- 1. Protocol Development / Medical Writing
- 2. Site Selection/ Start up/ Regulatory
- 3. Project Management
- 4. Clinical Monitoring
- 5. Data Management
- 6. Pharmacovigilance/ Safety
- 7. Medical Monitoring
From draft idea to full protocol and CSR
From initial site identification to country specific regulatory needs, TRS has successfully launched trials in 43 countries
Process driven project management to deliver key study milestones on time, every time
Vetted and therapeutically aligned clinical research associates who can are local language experts as well as primary site contracts throughtout lifecycle of trial
From database design and build to eCRF deployment and database lock, TRS has worked with multiple eCRF vendors to ensure a smooth deployment for both the sponsor and site
Safety database design , management and notification across the trial and globe per country regulations
24-hour therapeutically aligned physician management and leadership to ensure translational protocol adherement.