feedzop-word-mark-logo
searchLogin
Feedzop
homeFor YouUnited StatesUnited States
You
bookmarksYour BookmarkshashtagYour Topics
Trending
trending

IRS stimulus direct deposit rumors

trending

Nvidia: 'one team' culture

trending

Retirement income policies review

trending

Virus linked to lupus cases

trending

Telegram's Cocoon AI accelerates

trending

Bitcoin price drops below $100,000

trending

FIFA U-17 World Cup thrills

trending

Walmart CEO Doug McMillon retires

trending

Alibaba AI app relaunch planned

Terms of UsePrivacy PolicyAboutJobsPartner With Us

© 2025 Advergame Technologies Pvt. Ltd. ("ATPL"). Gamezop ® & Quizzop ® are registered trademarks of ATPL.

Gamezop is a plug-and-play gaming platform that any app or website can integrate to bring casual gaming for its users. Gamezop also operates Quizzop, a quizzing platform, that digital products can add as a trivia section.

Over 5,000 products from more than 70 countries have integrated Gamezop and Quizzop. These include Amazon, Samsung Internet, Snap, Tata Play, AccuWeather, Paytm, Gulf News, and Branch.

Games and trivia increase user engagement significantly within all kinds of apps and websites, besides opening a new stream of advertising revenue. Gamezop and Quizzop take 30 minutes to integrate and can be used for free: both by the products integrating them and end users

Increase ad revenue and engagement on your app / website with games, quizzes, astrology, and cricket content. Visit: business.gamezop.com

Property Code: 5571

Home / Health / Veteran Cancer Drug Regulator to Lead FDA's Main Drug Approval Division

Veteran Cancer Drug Regulator to Lead FDA's Main Drug Approval Division

13 Nov

•

Summary

  • FDA appoints Dr. Richard Pazdur, a respected cancer drug regulator, to lead the Center for Drug Evaluation and Research
  • Pazdur has been with the FDA for 26 years and is known for helping speed up approval of lifesaving cancer drugs
  • The FDA has seen hundreds of staff departures in the past year

In a move to stabilize the U.S. Food and Drug Administration (FDA), the agency has appointed one of its most respected cancer drug regulators, Dr. Richard Pazdur, to lead the Center for Drug Evaluation and Research (CDER). Pazdur, who has been with the FDA for 26 years, is taking on this new role at a time when the agency has faced significant upheaval, with hundreds of staff departures over the past year.

Pazdur is known for his work in helping speed the approval of lifesaving cancer drugs. His appointment to the helm of CDER, which oversees most prescription and over-the-counter drugs, is seen as a positive step forward for the agency. "I'm honored to lead CDER at a time when the FDA is achieving long-sought regulatory reforms," Pazdur said, expressing his enthusiasm to help the country "reach its peak in drug development."

The CDER has seen its staff numbers decline by around 1,000 this year due to dismissals, buyouts, and resignations. Pazdur's predecessor, Dr. George Tidmarsh, recently resigned after being placed on leave during an inspector general investigation. Tidmarsh, a former biotech executive, had faced criticism and a lawsuit over his handling of the FDA's fast-track approval system.

Disclaimer: This story has been auto-aggregated and auto-summarised by a computer program. This story has not been edited or created by the Feedzop team.
Dr. Richard Pazdur is a veteran cancer drug regulator who has been appointed to lead the FDA's Center for Drug Evaluation and Research, the agency's main division for approving new drugs.
The FDA has faced a turbulent year with hundreds of staff departures within the agency, leading to a decline of around 1,000 employees at the Center for Drug Evaluation and Research.
Pazdur has expressed his enthusiasm to help the country "reach its peak in drug development" in his new role leading the FDA's main drug approval division.

Read more news on

Healthside-arrow

You may also like

FDA Eases Biosimilar Approvals, but Patent Hurdles Remain

10 hours ago • 2 reads

article image

FDA Clears BrainsWay's Deep TMS System for Adolescent Depression Treatment

10 hours ago • 4 reads

article image

FDA Approves Rare Leukemia Pill Komzifti, Faces Boxed Warning

22 hours ago • 4 reads

Biocon Cuts Biosimilar Costs by 50% as US Eases Testing Rules

1 day ago • 5 reads

article image

ByHeart Recalls All Formulas Amid Botulism Outbreak

1 day ago • 70 reads

article image