AI Research Inc. Services

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

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