Prospects for Change at FDA Under the Trump Administration: Early View of What 2017 Will Bring

Instructor: Steven Grossman
Product ID: 705023
Training Level: Overview/ Basic
  • Duration: 90 Min
This webinar will discuss FDA's current priorities and the agency's likely priorities and the future of regulations and policies in 2017 under the new Trump administration.

recorded version

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Recorded Link and Ref. material will be available in My CO Section
Last Recorded Date: Dec-2016

Training CD / USB Drive

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CD/USB and Ref. material will be shipped within 15 business days

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Read Frequently Asked Questions

Why Should You Attend:

The US has a new president, a new Congress, and almost assuredly a new agenda for the FDA — with different policies and priorities than the current administration.

What does this mean for FDA regulated industries?

Steve Grossmann — a long-time D.C. insider, who served as a Senate Health Committee Staff Director and Deputy Assistant Secretary of Health — will discuss what the FDA is doing today and what it likely will be doing under the next administration.

Areas Covered in the Webinar:

After attending this 90-minute webinar you will learn:

  • The likelihood that the current commissioner will continue to head the agency —for how long — and who the top candidates are to replace him
  • Who will head the FDA transition team and how the process will likely unfold in the next months
  • What the FDA’s likely priorities will be in 2017 under the new administration besides the medical device tax and drug pricing and the signals you need to watch for to determine how the new policies will likely impact your company — and your job on a daily basis
  • How the new Congress is likely to impact what FDA does in 2017 and whether there will be increased monitoring of specific FDA projects, offices and policies

Who Will Benefit:

Anyone in position to lead an FDA regulated company, new product for regulatory approval or is concerned about trends in FDA regulation and policy will benefit from this webinar.

  • Senior Management (C-level, President, VP and Director level)
  • Regulatory Affairs
  • Product Management
  • Consultants
  • Attorneys
Instructor Profile:
Steven Grossman

Steven Grossman
President of HPS Group, LLC

Steven Grossman is President of HPS Group, LLC, a consultancy that provides strategic counsel, analysis and advocacy on regulatory and policy issues involving the U.S. Food and Drug Administration. Mr. Grossman serves on the Board of Directors of the National Organization for Rare Disorders (NORD) and sits on the board’s executive committee. He is also a founder and deputy executive director of the Alliance for a Stronger FDA, a multi-stakeholder coalition that advocates for increased resources for the FDA. Earlier in his career, Mr. Grossman was Deputy Assistant Secretary for Health at HHS and Health Staff Director and Counsel to the Senate HELP Committee.

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Refund Policy

Registrants may cancel up to two working days prior to the course start date and will receive a letter of credit to be used towards a future course up to one year from date of issuance. ComplianceOnline would process/provide refund if the Live Webinar has been cancelled. The attendee could choose between the recorded version of the webinar or refund for any cancelled webinar. Refunds will not be given to participants who do not show up for the webinar. On-Demand Recordings can be requested in exchange.

Webinar may be cancelled due to lack of enrolment or unavoidable factors. Registrants will be notified 24hours in advance if a cancellation occurs. Substitutions can happen any time.

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