Regulations.gov document

Content and Format of Substantial Equivalence Reports; Food and Drug Administration…

Rule · FDA-2016-N-3818 · posted Oct 5, 2021

Key facts

Document ID FDA-2016-N-3818-0176
Title Content and Format of Substantial Equivalence Reports; Food and Drug Administration Actions on Substantial Equivalence Reports
Document type Rule
Subtype Final Rule
Agency FDA
Docket FDA-2016-N-3818
Posted Oct 5, 2021
Federal Register citation FR 86 55224
FR document number 2021-21009
CFR 21 CFR Parts 16 and 1107
Comment period opens Oct 5, 2021
Effective date Oct 5, 2021

At a glance

  • 10–99 Pages
  • 100–999 Public comments on this docket

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