Abortion Pill Mifepristone Will No Longer Require In-Person Pick Up, US FDA Concludes

REMS modification implemented for the duration of the pandemic will become permanent, the agency determines in response to lawsuit. FDA adds a requirement that pharmacies dispensing the drug be certified.

Mifeprex
FDA lifts REMS restriction on use of abortion pill Mifeprex • Source: Alamy

The US Food and Drug Administration has bowed to calls that it do away with the requirement that the abortion pill Mifeprex (mifepristone) be dispensed to patients at a hospital, clinic, or medical office.

In response to a lawsuit filed by the American Civil Liberties Union, the agency reviewed its Risk Evaluation and Mitigation Strategy (REMS) for Mifeprex

Read the full article – start your free trial today!

Join thousands of industry professionals who rely on Pink Sheet for daily insights

  • Start your 7-day free trial
  • Explore trusted news, analysis, and insights
  • Access comprehensive global coverage
  • Enjoy instant access – no credit card required

More from Drug Safety

More from Pink Sheet

Recent and Upcoming FDA Advisory Committee Meetings

 
• By 

Recent and upcoming US FDA advisory committee meetings and a summary of the topics covered.

UK Health Data Research Service Looks ‘Encouraging’ For Industry, But Implementation Details Will Be Key

 

Marcus Vass and Vladimir Murovec of international law firm Osborne Clarke tell the Pink Sheet what the government's planned HDRS might mean for industry, and how it compares with the European Health Data Space.

EU Health Data Space May Speed Up R&D Through Access To Multi-Omics & Clinical Record Data

 

The European Health Data Space framework will allow companies to accelerate R&D processes and identify new molecular targets faster by facilitating centralized access to certain types of high-quality data, Finland’s Orion Pharma says.