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Research Site

5 reasons why becoming a CRA might be right for you

Clinical Research Associates (CRAs) also called clinical monitors or trial monitors are the ones who are responsible to oversee the clinical trials on behalf of the sponsor. They have several responsibilities including but not limited to Source Data Verification (SDV), Source Data Review (SDR), writing reports, scheduling monitoring visits, and…

Note to File in Clinical Studies

A Note to File (NTF) is a record that allows the clinical site and the sponsor to document an identified issue or discrepancy during a clinical study. A NTF should include the following items: ·     The root cause of the discrepancy/issue ·     The corrective action taken to prevent its recurrence ·     Explanation of…