AI Research Inc. Services


Areas of Expertise

On-Site & Remote Monitoring

  • Compliance with FDA GCP regulations
  • Compliance with ICH guidelines
  • Adherence to quality plans and systems
  • Experience with wide variety of EDC and CTMS systems

Clinical Trial Execution

  • Assist with Development of study protocol
  • Creation of study timelines
  • Creation of study budget
  • Creation of study support materials
  • Management of trial execution from pre-study evaluation visits through site close out visits and final study report

Fact Sheet Download

AI Research Fact Sheet