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What’s Next? Webinar, Sept. 27, 2019

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FALLS CHURCH, Va. (PRWEB)

FDA and EU Inspections

The Mutual Recognition Agreement: What’s Next?

**An FDAnews Webinar**

Friday, Sept. 27, 2019, 1:30 p.m. – 3:00 p.m. EDT

https://www.fdanews.com/fdaeuinspect

Who’s that knocking on the door? The FDA … or someone else?

Don’t rule out ‘someone else.’ Under the new Mutual Recognition Agreement (MRA), investigators from any of the 28 EU member states have the right to inspect global drugmakers’ operations.

And foreign inspectors may be the least of the company’s concerns. Now that the MRA is fully implemented at last, companies face new issues including: pros and cons of relying on EU inspections, potential for increased efficiency across the board, and next steps as the U.S. and EU enter a new era of cooperation.

Compliance consultants Cynthia Schnedekar Esq. and Elizabeth (“Liz”) Oestreich Esq. are the guides for a 90-minute survey of the post-MRA world. Attendees will discover:


  • MRA Timeline: The Food and Drug Administration Safety and Innovation Act (FDASIA) of 2012 and what it has led to

  • Benefits so far: How inspectors are using each other’s inspections to maintain a risk-based approach … potential benefits for U.S. drug safety

  • And costs: How the MRA may complicate regulatory and compliance operations … which inspections FDA will continue to perform … which will go to EU member states

  • What’s next for: FDA capability assessments … possibility of duplicating the MRA model in other regions … potential impact of ‘Brexit’ on the MRA

Full implementation of the MRA only took place this July so there’s still lots to learn. If the organization sells drugs into EU nations — or anywhere in this interconnected world — one will want to mark the calendar for this timely presentation.

Interested in registering multiple sites?

Call (888) 838-5578 in the U.S. or +1 (703) 538-7600 globally

to learn about our special multisite discount.

Webinar Details:

FDA and EU Inspections

The Mutual Recognition Agreement: What’s Next?

**An FDAnews Webinar**

Friday, Sept. 27, 2019, 1:30 p.m. – 3:00 p.m. EDT

https://www.fdanews.com/fdaeuinspect

Tuition:

$287 per site

Easy Ways to Register:

Online: https://www.fdanews.com/fdaeuinspect

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.

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