Clinical Study Process Optimization

Comprehensive clinical services and technology solutions to help life science companies of all types and sizes manage their entire clinical operations process - from Phase I through regulatory submission.

Clinical trial processes can be labor intensive, that’s why we offer cost efficient solutions to streamline operations through all phases of development. From clinical user acceptance testing and validation services to faster study start-up through the use of clinical portals, USDM can provide the level of support you need to successfully manage your clinical study.

Key Services:

  • Study Specific User Acceptance Testing (EDC, IVRS, and ePRO)
  • Clinical and Investigator Portal Solutions
  • Process Analysis, Improvement and Management for Clinical Operations
  • Clinical Database Programming
  • Clinical Systems Integration & System Validation
  • Programming/Business Analysis
  • Solution and Service Vendor Requests, Vendor Selection, and Third-Party Contracts
  • SAS Programming | Biostatisticians Support
Thought Leaders

Leading experts in every Life Sciences field.

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Bob Lucchesi

Vice President of Global Regulatory Compliance, Quality Assurance and Auditing

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