Medical Device Regulations Conference

Starts:  Nov 7, 2017 07:30 (ET)
Ends:  Nov 8, 2017 17:00 (ET)
Associated with  Atlanta Chapter

Early Bird Registration Now Available!

The only annual medical device regulations conference in the Southeast that offers industry expert speakers, an intensive one day workshop, and six hours of RAPS continuing education credit. This program offers a packed agenda and a great opportunity to gain exposure to current thinking and best practices regarding medical device quality and regulatory affairs from both industry and FDA management.

Register 3 people and earn an additional FREE registration!
Early registration discounts are available through September.

Dates: November 7-8, 2017
Location: Lawrenceville, GA (near Atlanta)
Claim Your Discount
Co-sponsored by the FDA and a top public research university, this conference is of special interest to QA and RA professionals. Please join the University of Georgia and the US Food and Drug Administration for the 5th annual Medical Device Regulations Conference & Workshop this November at the University of Georgia’s Gwinnett Campus in Lawrenceville, Georgia.

The Workshop - MDSAP

On November 7th, spend your day getting expert advice on implementing the Medical Device Single Audit Program with ISO 13485: 2016 considerations that will help you lead your organization to an MDSAP compliant QMS. Seats are limited –reserve yours today.

MDSAP is an international initiative led by five Regulatory Authorities to implement a program where Auditing Organizations can conduct a single audit of a medical device manufacturer that would be accepted by multiple regulators internationally to address QMS/GMP requirements.
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