1. Pink Sheet
  3. >>US FDA

Will US FDA Wind Up With More Political Positions Under Trump?

 
• By Derrick Gingery

Incoming administration could appoint key legal and policy positions to shape agenda’s agenda.

FDA entrance sign 2016

As President-elect Trump's transition continues, FDA soon will find out whether his influence will stretch deep inside the agency. High level policy and legal positions that have been filled with career FDA staff could become administration appointees in part to ensure the agency is in line with Trump's and HHS Secretary nominee Tom Price's agendas.

Marc Scheineson, head of the food and drug law practice at Alston and Bird and former FDA associate commissioner for...

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
Start Free Trial

Already a subscriber?

More from US FDA

US FDA Requires Opioid Class Labeling Changes Despite Adcomm Advice

 
• By Kate Rawson

Quantitative estimates of the safety risks with opioid pain medication, including the risk of addiction and misuse, must be added to labeling.

US FDA Skips User Fee Increase For More Staff Amid Exodus, Hiring Difficulties

 
• By Derrick Gingery

A calculation used to determine whether the FDA has the staff to handle its workload also was not included in the description of prescription drug user fee calculations.

New US FDA Chief Counsel More Familiar With Trump World Than Food and Drug Law

 
• By Sarah Karlin-Smith

Sean Keveney is largely unknown in the FDA law space, but likely is familiar and connected to the White House given his work on Trump’s antisemitism taskforce.

Will US FDA’s Leadership Rediscover The Value Of Advisory Committees?

 
• By Michael McCaughan

After the abrupt departure of CBER’s director, it seems FDA, and Vinay Prasad in particular, would likely have been well served by hearing from an advisory committee before requesting the suspension in sales of Sarepta’s DMD gene therapy Elevidys.

More from Agency Leadership