what we can do.

clinical study management

  • Blinded or Unblinded Study Management

  • Vendor management

  • Study document and manual review with editing

  • Protocol deviation review

  • Monitoring Visit Report review

    Snapshot of capabilities, not an exhaustive list

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tmf management

  • eTMF Audit readiness

  • eTMF QC and issue resolution

  • eTMF Report review to ensure compliance with filing guidelines and SOPs 

    Snapshot of capabilities, not an exhaustive list

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study start up

  • Feasibility and site selection management

  • Site activation projections

  • Site activation activities tracking

  • SIV and site training preparations

    Snapshot of capabilities, not an exhaustive list

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