Library / Laws / 113th Congress / House Bills / H.R. 4918
H.R. 4918
To require the Food and Drug Administration to expedite review of pharmaceuticals that are approved for marketing in the European Union.
| Print stage | Date | Size | ⠃ |
|---|---|---|---|
| Introduced in House | 2014-06-19 | 1.4K | ⠃⠗⠋ |