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Counselor Education Program & I Clinical DocumentationS ite Agreement FormInstructions: Complete the information in the fields provided below. Review form upon completion and sign. Return completed
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What is P & I Clinical Documentation - Site Agreement - education ufl Form?

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P amp i clinical refers to the Pharmacovigilance and Risk Management Plan for clinical trials.
The sponsor of the clinical trial is required to file the p amp i clinical.
The p amp i clinical should be filled out by providing detailed information on pharmacovigilance activities and risk management strategies for the clinical trial.
The purpose of the p amp i clinical is to ensure patient safety during the clinical trial and to minimize risks associated with the investigational product.
The p amp i clinical should include information on safety monitoring, adverse event reporting, risk assessment, and risk minimization measures.
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