Regulations.gov document

Significant Risk and Nonsignificant Risk Medical Device Studies: Guidance For IRBs…

Other · FDA-2006-D-0031 · posted Jan 1, 2006

Key facts

Document ID FDA-2006-D-0031-0005
Title Significant Risk and Nonsignificant Risk Medical Device Studies: Guidance For IRBs, Clinical Investigators, and Sponsors
Document type Other
Subtype Guidance
Agency FDA
Docket FDA-2006-D-0031
Posted Jan 1, 2006
Comment period opens Jan 1, 2006

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