FDA's New Commissioner under Trump's Administration: The way forward for the FDA

Duration: 60 Minutes
How will the FDA change under the Trump administration and the new FDA Commissioner? This event will explore the implications of the Trump Administration and President Trump's pick of Dr. Scott Gottlieb as new FDA Commissioner and Tom Price as Secretary of Health & Human Services on the future of the FDA. The event will cover Trump's regulatory agenda, his deregulation task force at federal agencies and his proposed budgetary cuts. Trump's new pick for commissioner of the FDA will be discussed in detail as well as his intention to ease drug regulations and streamline the agency and the drug approval process.
Trump Administration
Instructor: Norma Skolnik
Product ID: 507019
Objectives of the Presentation
  • To learn about President Trump's regulatory agenda
  • To understand how the Congressional Review Act may impact the FDA
  • To gain an understanding of Trump's intentions for the drug & device approval process
  • To learn about Tom Price, the new head of Health & Human Services
  • To learn about Dr. Scott Gottlieb, the new FDA Commissioner and how he may influence the FDA
Why Should you Attend
Anyone interested in the workings of the FDA and how the agency may be impacted by the Trump administration and the new FDA commissioner could benefit from this presentation.

Areas Covered
  • President Trump's stated goal to overhaul the Food and Drug Administration
  • Trump's intentions to upend and streamline the drug approval process
  • Dr. Scott Gottlieb, Trump's new pick for FDA Commissioner, and his potential influence on FDA What Gottlieb's recent Senate confirmation hearing reveals about his ideas
  • HHS Head Tom Price and past policies that he's supported: Price's intentions for HHS programs
  • Trump's proposed budget cuts, regulatory restrictions & the FDA
  • Potential risks of deregulation for drugs and other FDA regulated products
  • Industry reactions to Trump's call to cut regulations and streamline the agency
Who will Benefit
Regulatory Affairs managers, directors & associates, Research & Development managers, Compliance Specialists, Drug and Food labeling managers, Marketing managers and anyone involved in marketing Prescription drugs and OTC drugs, medical devices, biologics or foods in the U.S.
$375
Recorded Session for one participant
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  • Get answers to your queries through interactive Q&A sessions via chat at the end of the session
  • Download the Certificate of Attendance and Purchase Invoice from your OCP Account 24 hours after the completion of the session
  • Please let us know your thoughts and views at the end of the webinar, your valuable feedback will help us improve
Recorded Session - How it works
  • Login to onlinecompliancepanel with your registered username and password https://www.onlinecompliancepanel.com/login
  • Upon purchase of the recorded session a link will be updated on your OCP Account within 24 hours
  • Please click on the link to access the Recorded Session
  • Presentation handouts in downloadable PDF format will be updated on your OCP Account within 24 hours of the purchase of the product
  • Download the Certificate of Attendance and Purchase Invoice from your OCP Account after 48 hours of the product Purchase
  • Please share your valuable Feedback at the end of the session
Instructor Profile:
Norma Skolnik works as a regulatory consultant to FDA regulated companies and to firms who wish to launch products in the U.S.A. Norma has over 35 years of U.S. regulatory experience, starting in the pharmaceutical industry. She was the Associate Director of Regulatory Affairs at Lederle Laboratories in Pearl River, N.Y. and then became Associate Director of Regulatory Affairs at Lederle Consumer Health where she helped launch Centrum and Caltrate dietary supplements. When Lederle was acquired by Wyeth, she became Associate Director of Regulatory Affairs there, acquiring more experience in the Dietary Supplement and OTC drug fields. She joined Warner-Lambert Consumer Health division in 1998 and became Assistant Director of Adams Regulatory Affairs. In 2002, when Pfizer acquired Warner Lambert she was promoted to Director of Regulatory Affairs for the Adams division. Adams was acquired by Cadbury-Schweppes in 2003 and she served as Cadbury Adams' Director of Regulatory Affairs for the Americas from 2003 until her retirement in 2008.

Norma earned a Bachelor's degree in Biology from the University of Cincinnati and holds a Master's degree from Pratt Institute in Brooklyn, New York. She's also done graduate work at Columbia University and Montclair State University.
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