Site Monitoring
FRS’ experienced monitors can perform investigational site visits for study start-up, interim site visits and study closeout site visits to validate and verify data collected at/by the site. We will create a monitoring plan in coordination with you to define the scope and frequency of the clinical site monitoring.
Our clinical monitors also can provide assistance with reporting and management of adverse events; support the investigational site during an inspection by regulatory authorities and provide in-house review of study documentation.
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