ITHS offers clinical study monitoring to help investigators who are required by FDA or their funding agency to have ongoing independent review of their research records.
ITHS monitoring services helps clinical investigators to:
Maintain compliance with international, federal, state, local, institutional, and protocol-driven regulatory requirements for clinical research
Ensure the accuracy of research data, including source document verification, confirmation of participant eligibility, and adverse event identification
Monitoring services can be provided in-person or remotely. ITHS provides monitoring services upon request on a fee for service basis. For more information or to request a price quote, please contact us.
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