NIH SCIENTIFIC FRAUD INVESTIGATOR WALTER STEWART

NIH SCIENTIFIC FRAUD INVESTIGATOR WALTER STEWART is on temporary detail to Chairman Dingell's (D-Mich.) House Oversight & Investigations Subcommittee staff. Stewart has been with the subcommittee for about eight months, joining shortly after he appeared at April subcommittee hearings. Stewart's stint with the subcommittee is open-ended. Stewart testified at the subcommittee's April hearings as an expert in the area of uncovering scientific misconduct. For nearly five years, Stewart and NIH colleague Ned Feder, MD, have been involved in researching the accuracy of scientific literature and of scientific misconduct, particularly in NIH-supported research. The two published an article in Nature Jan. 15, 1987, analyzing alleged errors and discrepancies in 18 papers by cardiology researcher John Darsee and co-authors. Stewart and Feder have also written about a study done at MIT and co-authored by Nobel prize-winner David Baltimore. Stewart and Feder are with the National Institute of Diabetes and Digestive and Kidney Diseases. In other cases, the subcommittee is looking into a study done by a former Harvard researcher on the use of a vitamin A (tretinoin) ointment for dry eye syndrome and into the use of diagnostic procedures developed by Duke University scientists.

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 Archive

Ocaliva: Still No Clarity On Why EU Court Opposed Revocation Of Approval

 

Advanz Pharma would have had to show that the European Commission’s decision to revoke Ocaliva’s conditional marketing approval risked causing serious and irreparable harm, according to lawyers from Van Bael & Bellis.

Final Chance To Have Your Say: Take Our Reader Survey This Week

 
• By 

This is your final call to participate in the survey to better understand our subscribers’ content and delivery needs. The deadline is 20 September.

Shape Our Content: Take The Reader Survey

 
• By 

We are conducting a survey to better understand our subscribers’ content and delivery needs. If there are any changes you’d like to see in coverage topics, article format, or the method in which you access the Pink Sheet – or if you love it how it is – now is the time to have your voice heard.

Brazil Pilots Digital Drug Pack Inserts

 

A new pilot aims to take Brazil closer to ‘digital transformation.’

More from Pink Sheet

US FDA Asking Questions About Commissioner’s Voucher Program With Details Scarce

 

FDA staff are trying to plan for program implementation in the absence of critical eligibility and other details, although guidance may be coming soon.

Senate Appropriators Give US FDA More Non-User Fee Funds Than House

 

US FDA would receive more funding for fiscal year 2026 in the Senate appropriations bill than its House counterpart, including $10m for unannounced foreign inspections.

EU Medical Countermeasures Strategy Promises More AMR Pull Incentives

 

A new EU strategy to ensure access to essential medicines will boost the development of critical medical counter measures, including vaccines and therapies, according to one pharmaceutical industry group.