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The Multisite Trials Coordinating Center (MTCC) integrates a Trial Coordinating Center (TCC) and a Data Coordinating Center (DCC) to advance excellence in multisite clinical trials. By bringing together complementary expertise in clinical coordination, methodology, operations and data coordination, the MTCC partners with investigators to design, coordinate, conduct and disseminate innovative, rigorous and impactful multicenter studies.

Graphic for MTCC Clinical Study Support life cycle nad this image establishes the following: 1.Proposal DevelopmentFunding ApplicationRegulatory Risk Review, 2. IntakeOperational ReviewsData Management StrategyRegulatory Strategy Checks, 3. Protocol DevelopmentStatistical ConsiderationsRandomization and Blinding, 4.  ImplementationCase Report Forms (CRFs)Data Standards and DerivationsDSMB Charter, 5. Pre-LaunchRegulatory Submission and ApprovalDetailed DMP, DQP, 6. LaunchSAP and TFL ShellsDry-Run and ReadinessDSMB Open Session Report, 7. Report and Close-OutSAP and Database LockFinal ReportsRegulatory SubmissionSupport