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Stanford University Internal Use Only Research Compliance Office Human Subjects ResearchSponsorInvestigator Checklist IDE (Devices) This checklist is based on the Sponsor and Investigator responsibilities
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The sponsor-investigator checklist IDE devices is a document used to ensure that the sponsor-investigator complies with FDA regulations when conducting an investigation of a new medical device.
The sponsor-investigator is required to file the sponsor-investigator checklist IDE devices.
The sponsor-investigator checklist IDE devices should be filled out by providing all necessary information and ensuring compliance with FDA regulations.
The purpose of the sponsor-investigator checklist IDE devices is to ensure that the sponsor-investigator follows all necessary protocols and regulations when conducting an investigation of a new medical device.
The sponsor-investigator checklist IDE devices must include information on the investigation plan, device specifications, risk assessment, and other relevant details.
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