l9n/ New Jersey

2016–2017 Session

Senate Bill 2024

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.

Became P.L.2016, c.73, on December 5, 2016.

Sponsors

Who carried the bill in each chamber, and who signed on. Each name leads to the member's page.

In the Senate

In the General Assembly

2 co-sponsors

Declan J. O'Scanlon Jr., Nancy J. Pinkin

Its course

April 18 to December 5, 2016, on one scale. In the top row each mark is a day something happened; taller marks are busier days.

Each committee stop sits inside its chamber.

Every action8 actions on 6 days

In the SenateApr 18 to Jun 3073 days

In the General AssemblyJun 30 to Oct 20112 days

Health and Senior ServicesJun 30 to Oct 698 days

With the GovernorOct 20 to Dec 546 days

Votes

Yeas to nays, as the Legislature recorded them. Committee votes are set in.

  • Senate, third reading40–0

    Passed · Jun 30

  • General Assembly, third reading73–0

    Passed · Oct 20

Text

Each version as the Legislature printed it.

l9n doesn't hold this bill's text yet.

What happened

In l9n's words, one line for each step. Every action as the Legislature published it is below.

In the Senate Apr 18 – Jun 30

  1. Introduced in the Senate and sent to Health, Human Services and Senior Citizens
  2. Health, Human Services and Senior Citizens recommended it
  3. Read a second time
  4. Passed the Senate, 40 to 0

In the General Assembly Jun 30 – Oct 20

  1. Arrived in the General Assembly
  2. Sent to Health and Senior Services
  3. Health and Senior Services recommended it
  4. Read a second time
  5. Passed the General Assembly, 73 to 0, and so both houses

To the Governor Dec 5

  1. Signed by the Governor
  2. Became P.L.2016, c.73
All 8 actions, as published