Announcing the 2016 FDA Regulatory 101 Series

Medical device professionals in Ohio, are you ready?

Last year R&Q teamed with BioOhio to present an ongoing series of 101 medical device events throughout the year. Thanks to participation and feedback from ambitious medical device professionals across Ohio - and the support of our gracious hosts - the events were a success. Because of that, we're thrilled to announce we'll be presenting a new and improved program in 2016! One webinar and three in-person events are on tap for this year, with the first - a webinar on medical mobile apps - scheduled for March 3, 2016. Register for the webinar and see the list of upcoming FDA Regulatory 101 events below.

FDA Regulatory 101 Series Webinar: Medical Mobile Apps
Thursday, March 3, 2016
11:30am - 12:30pm EST

The webinar will focus on app development for the medical, health, and life science industries. In this webinar, R&Q will explain when your app may be classified as a medical device in the eyes of the FDA and other regulatory bodies. If your app does fall under regulation, we’ll also give you a step-by-step guide to move your concept to a legally marketed medical device. This webinar is open to both members and non-members of BioOhio.

Each session of the FDA Regulatory 101 Series covers a spotlight topic along with basic regulatory and quality principles. This cost-effective series is geared toward small and start-up companies, junior regulatory and quality staff, medical device development and manufacturing staff, yet is still appropriate for seasoned regulatory and quality professionals wishing to brush up on current trends and expectations.

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FDA Regulatory 101 Series - Cincinnati
Tuesday, May 10, 2016
Host: Stress Engineering Services
Agenda to be announced
Register here

FDA Regulatory 101 Series - Columbus
Thursday, July 28, 2016
Host: Battelle
Agenda to be announced
Register here

FDA Regulatory 101 Series - Cleveland
Thursday, October 27, 2016
Host: TBD
Agenda to be announced
Register here

“We believe events like this are critical to Ohio’s success. Regulatory and quality gatherings in our own state are one way we can get a leg up on medical device hubs like Boston, Minnesota, and Southern California. Practical knowledge of quality and regulatory topics helps start-ups and small companies become both compliant and efficient, and large companies build and maintain internal expertise. With the combination of the BioOhio FDA Regulatory Forum, the FDA Regulatory 101 Series, and MedCon, Ohio is building a strong medical device quality and regulatory foundation that benefits all of us!”
– Chad Gibson, R&Q Project Engineer