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  • ENGLISH
  • FRANCAIS
  • Services
    • Services Overview
    • Clinical Trial Operations
      • Protocol Development and Study Design
      • Feasibility and Study Start Up
      • Patient Recruitment
      • Project Management
      • Clinical Operations
      • Centralized Monitoring
      • Decentralized Clinical Trials (DCT)
      • Centralized eTMF
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    • Regulatory and Drug Development Consulting
      • Clinical Strategy
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      • Chemistry, Manufacturing, and Controls (CMC)
      • Regulatory Affairs
      • GxP Strategy Consulting
      • Publishing and Submissions
      • Medical Writing
    • Government and Public Health Services
    • Biometrics
      • Biostatistics and Statistical Programming
      • Data Management
    • Clinical Pharmacology Modeling Simulation
      • Clinical Pharmacology Integrated Drug Development
      • Model Informed Dose & Drug Development (MIDD)
      • Pharmacometrics (PMx), Pharmacokinetics, Pharmacodynamics (PK/PD)
      • DMPK and Translational Discovery and Development
  • Therapeutic Expertise
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Centralized eTMF

  • Clinical Trial Operations
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  • Centralized Monitoring
  • Decentralized Clinical Trials (DCT)
  • Centralized eTMF
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    • Medical Monitoring
    • Pharmacovigilance and Patient Safety
    • Therapeutic Oversight

The Electronic Trial Master File (eTMF) centralizes all information about the clinical trial, documentation of trial conduct, and reporting of trials. Our eTMF experts at Allucent are equipped with advanced processes from TMF setup to end-of-study TMF delivery.

Allucent has implemented the Veeva Vault eTMF to provide our clients and study teams with a platform that ensures a constant state of inspection readiness, increased visibility, oversight, and collaboration. 

Contact Us

Let us partner with your team on bringing new therapies to light. Get in touch to get started.

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