Medical Devices 101: An Educational Forum- Oklahoma City, Oklahoma
We are pleased to announce Medical Devices 101: An Educational Forum on Juyl 26, 2013. Because there is a limited capacity for this event, we recommend advanced registration. Register Now
Download Presentation- Device 101 July 2013
Location
Moore Norman Technology Center
13301 s. Pennsylvania
Oklahoma City, OK 73170
Date and Time
Friday, Jul 26, 2013
08:00 AM – 05:00 PM Central
Description
This educational forum is intended for folks with little to no experience with FDA requirements for medical device manufacturers, specification developers, and initial distributors of imported devices. It is particularly useful to entrepreneurs, very small start-up companies, new hires, students planning a career in the medical device industry or enforcement, and administrative and marketing employees in medical device firms.
The Food and Drug Administration is responsible for regulating firms who manufacture, repackage, relabel, and/or import medical devices sold in the United States. Medical devices are classified into Class I, II, and III. Regulatory control increases from Class I to Class III. The device classification regulation defines the regulatory requirements for a general device type. Most Class I devices are exempt from Premarket Notification 510(k); most Class II devices require Premarket Notification 510(k); and most Class III devices require Premarket Approval.
The basic regulatory requirements that manufacturers of medical devices distributed in the U.S. must comply with are:
– Establishment registration,
– Medical Device Listing,
– Premarket Notification 510(k), unless exempt, or Premarket Approval (PMA),
– Investigational Device Exemption (IDE) for clinical studies
– Quality System (QS) regulation,
– Labeling requirements, and
– Medical Device Reporting (MDR)
Medical Devices 101 provides a brief overview of all of the above to folks new to the medical device industry.
Speakers
Al Alonso representing the industry viewpoint.
Dr. John Criscione, Biomedical Engineering professor, Texas A&M.
Lauren Skokan, FDA Consumer Safety Officer, Dallas District.
Dress Code
Business Casual
Contact
Sue Thomason, Secretary, FDMIC, Inc.
Price
Early Registration (registration will open on May 26, 2013) US$ 75.00
Regular Registration (registration will open on May 26, 2013) US$ 100.00
