Library / Laws / 114th Congress / House Bills / H.R. 1576
H.R. 1576
To require a study by the Government Accountability Office (GAO) to assess the Food and Drug Administration’s current regulatory pathway for reviewing generic versions of nonbiologic complex drug products, and for other purposes.
| Print stage | Date | Size | ⠃ |
|---|---|---|---|
| Introduced in House | 2015-03-24 | 9.6K | ⠃⠗⠋ |