Comprehensive site management and monitoring services ensure trials are conducted smoothly, safely, and in compliance with regulations. Our comprehensive site Management & Monitoring process involves:

  • Site identification and qualification
  • Feasibility studies
  • Site staff training
  • Document management
  • On-site monitoring
  • Remote monitoring
  • Risk-based monitoring
  • Source data verification (SDV)
  • Clinical trial material accountabilityRegulatory compliance
  • Audit preparation and support
  • Adverse event reporting
  • Safety management
  • Site close-out
  • Final reporting

Through these site management processes, we’re able to ensure you deliver accurate, high-quality data avoiding unnecessary roadblocks or delays in the drug development process.

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MSA News & Insights

What’s going on at Mesa and in the pharmaceutical world at large? Explore this section to find out!

Intern of the Week: Kaitlyn Wylie

Hood College is the educational institution of choice for over 2,000 students in and around Frederick, MD. Many of those…

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Mesa Science Associates and MedSurgPl Join Forces to Offer Convenience and Capability to Startup Biotech Firms

Frederick, MD – Mesa Science Associates, Inc. (MSA) and MedSurgPI, LLC have announced a partnership between their two companies, which…

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Internship Experience Reflection – Kaitlyn Wylie

I never thought my first job would be in the biotechnology and pharmacy industry, let alone with such a passionate…

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