Bill Texts: NJ S2024 | 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 7-3)

Status: (Passed) 2016-12-05 - Approved P.L.2016, c.73. [S2024 Detail]

Bill Drafts

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Chaptered2016-12-30HTML/TextLinkView
Introduced2016-04-18HTML/TextLinkView

Amendments

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No bill amendments currently on file for New Jersey S2024

Supplemental Documents

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No supplemental documents for New Jersey S2024 currently on file.

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