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Sponsor's Responsibilities
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Item Number: NWRR3015
A 17-page procedure that describes the responsibilities of the sponsor of a clinical trial and includes: protocol development and amendments; SOPs; investigator, monitor, study site, and CRO selection; IRB interaction; test article handling; data review and handling; reporting requirements; and trial termination/suspension. This procedure applies to all clinical trials for an investigational drug, biologic, or device that involves human subjects.
*Order 10 or more SOPs and get 10% off your order
*Order ALL 92 SOPs and get 25% off your order
*discount will automatically apply at checkout
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