FDAnews Announces: Medical Device Regulation in 2017: Crossroads Ahead?, Dec. 1, 2016, Washington, DC

Share Article

There’s going to be a new Administration and a new Congress in 2017 and, ready or not, there’s going to be new FDA regulations and guidances on medical devices as well as important legal decisions that will affect job responsibilities on a daily basis. This FDAnews Summit is completely interactive — no slides— just questions, answers and discussion among keynoter, moderators, panelists and attendees.

Medical Device Regulation in 2017:
Crossroads Ahead?
**Presented by FDAnews**
Dec. 1, 2016 – Washington, DC
http://www.fdanews.com/mdregulationin2017

Get ready for what 2017 holds.

There will be a new president, a new congress and new medical device regulations and guidances.

Come to the Press Club on December 1 and get a preview of what is coming.

Attendees will hear directly from former FDA officials including Herbert Lerner, Heather Rosecrans, Minnie Baylor-Henry, Mary Pendergast, Casper Uldriks — and many other experts and veteran practitioners in medical device regulatory issues who have been or are now on the firing line of the current hot button issues in medical device law, regulation, and policy: cybersecurity, mobile apps and combination products.

Not only will this be the first event of its kind after the election but it’s different. This FDAnews Summit is completely interactive — no slides— just questions, answers and discussion among the keynoter, moderators, panelists and the attendees.

Meet the Keynote Speaker:
Herbert Lerner, M.D., Senior Director of Regulatory and Clinical Sciences Hogan Lovells LLP
Herb Lerner's practice focuses primary on bringing new medical devices to the U.S. market. Uniquely positioned to advise clients in addressing FDA regulatory issues, he brings to Hogan Lovells years of clinical practice and FDA regulatory experience. A clinician with almost 20 years as a general and colon & rectal surgeon, and former Deputy Division Director of the Division of Reproductive, Gastro-Renal, and Urological Devices, FDA/CDRH/ODE, Herb joined the Hogan Lovells Medical Device Group in 2016.

Who Will Benefit:

  • Quality Assurance/Quality Control
  • Manufacturing and Contracting
  • Supply Chain Management
  • Risk Management and Product Lifecycle Management
  • Executive Management
  • Regulatory Affairs
  • Research and Development
  • Compliance Officers
  • Consultants/Service Providers

Conference Details
Medical Device Regulation in 2017:
Crossroads Ahead?
**Presented by FDAnews**
Dec. 1, 2016 – Washington, DC
http://www.fdanews.com/mdregulationin2017

Tuition: $697
Significant team discounts are available.

Easy Ways to Register
Online: http://www.fdanews.com/mdregulationin2017
By phone: 888-838-5578 or 703-538-7600

About FDAnews
FDAnews is the premier provider of domestic and international regulatory, legislative, and business news and information for executives in industries regulated by the US FDA and the European Medicines Agency. Pharmaceutical and medical device professionals rely on FDAnews' print and electronic newsletters, books and conferences to stay in compliance with international standards and the FDA's complex and ever-changing regulations.

Share article on social media or email:

View article via:

Pdf Print

Contact Author

Michelle Butler
FDANEWS
+1 (703) 538-7665
Email >
FDAnews
Like >
Visit website