Comments: NJ A3793 | 2016-2017 | Regular Session
Bill Title: Clarifies that product approval from U.S. Food and Drug Administration is not required for drug manufacturer to file registration statement, and specifies timeframe by which DOH must review registration statements.
Spectrum: Slight Partisan Bill (Democrat 6-2)
Status: (Introduced - Dead) 2016-10-20 - Substituted by S2024 [A3793 Detail]
Text: Latest bill text (Introduced) [HTML]
Spectrum: Slight Partisan Bill (Democrat 6-2)
Status: (Introduced - Dead) 2016-10-20 - Substituted by S2024 [A3793 Detail]
Text: Latest bill text (Introduced) [HTML]
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