What to Expect From FDA in 2019

Event Information
Product Format
Prerecorded Event
Presenter(s)
Conference Date
Tue, Dec 11, 2018
Length
60 minutes
Product Description

Get the Inside Scoop on What Will Likely Impact Your Business in 2019


The FDA is taking a fresh look at how to improve its gold standard for product review and consumer protection in 2019. It is therefore important that you know what to expect from the FDA in the second year of the Trump administration, and how this will likely impact your drug and medical device products. Doing so will not only prepare you in advance for the forthcoming changes, but also keep you one step ahead of the competition.

Learn what to expect from the FDA in 2019 in this webinar by industry expert Norma Skolnik. Skolnik will provide special insight on topics you may not find elsewhere on the market – such as the likely trends and changes to be expected from the FDA in the coming year; what new legislation will impact the pharmaceutical and consumer healthcare industry in 2019, and how the new FDA initiatives will impact the U.S. opioid crisis.

After attending this webinar, you will know the likely changes, trends, and legislations to expect from the FDA in 2019 – including how they will impact your industry. You will also be better informed about the FDA’s new steps in confronting the opioid crisis.

Session Highlights

This webinar will bring you up to speed with key areas, such as:

  • What are the likely trends and changes to be expected from the FDA in 2019?
  • What new legislation will impact the pharmaceutical and consumer healthcare industry?
  • How will FDA’s new initiatives impact the U.S. opioid crisis?
  • And more!

Who Should Attend

  • Regulatory affairs managers, directors and associates
  • Pharmaceutical product and marketing managers
  • Consumer healthcare marketing managers
  • Lawyers in the pharmaceutical and consumer healthcare industries

Ask a question at the Q&A session following the live event and get advice unique to your situation, directly from our expert speaker.

Order Below or Call 1-866-458-2965 Today

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Phone

1-866-458-2965

Fax

1-919-287-2643

About Our Speaker

Norma Skolnik - FDA Regulations Expert

Norma Skolnik has over 35 years of regulatory experience working with the pharmaceutical and dietary supplement industries. She served as Director of Regulatory Affairs for the Americas for Cadbury Adams. Prior to that, she was Director of Regulatory Affairs for the Adams Division of Pfizer and Associate Director of Regulatory Affairs for the Warner-Lambert company. She also served as Director of Regulatory Affairs for Lederle Consumer Healthcare and...   More Info
More Events By The Speaker

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