Brochure | May 2, 2022

In The Fight To Bring Innovative Therapies To Patients

Source: Worldwide Clinical Trials
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Building risk assessments and monitoring plans that focus on what is important into trial design lays the groundwork for a successful drug program by increasing data integrity and safeguarding patients. Our risk-based quality management (RBQM) capabilities ensure that:

  • Risks to critical data and processes are identified early
  • Functional areas each have unique and defined monitoring strategies
  • A validated, closed system (TRI OPRA) manages the process with access control and a full audit trail
  • A risk log that gives the option to add integrated forward looking indicators for Central Monitoring of potential risks in near real time

Download the available brochure to learn more.


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