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.