Medical Device Safety Conference: Regulations, Reporting & Tracking, 27-28 August 2012, Baltimore, MD

Main Category: Conferences
Article Date: 18 Jul 2012 - 5:00 PDT

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This summer in Baltimore, MD, regulatory and quality executives from all areas of the medical device industry will convene, sharing their insights into product safety. As medical technologies continue to grow in complexity and dynamics, the need to track and measure the safety of these products in both the short and long term has also increased. Recent high-profile cases of medical device safety issues both in Europe and the United States are driving regulators, politicians and the public to consider how the best manage and track device safety, while encouraging innovation and new product development.

Companies must remain up to date with regulatory trends, updates and changes in order to maintain both current and future compliance. The Medical Device Safety Conference agenda will discuss the present and future of safety with comprehensive programming over the event's two days, including sessions on unique device identifiers - post-market surveillance and traceability, adverse event reporting in today's regulatory landscape, recognizing industry trends to support the development of adequate safety policies and procedures and many more of safety's most pressing topics.

Risk management and post-market surveillance are critical responsibilities of regulatory and quality affairs teams, requiring them to forecast and track a product's current and future activity. Q1 Productions' Medical Device Safety Conference will cover all areas and responsibilities that come with medical device safety with a variety of group presentations, panel discussion and time set aside to network informally. For full details and/or registration, visit http://www.q1productions.com/devicesafety

Presenting Organizations to include: Food and Drug Administration's Office of Surveillance and Biometrics, ACell Inc., Becton Dickinson, GE Healthcare, Insulet Corporation, Kinetic Concepts, Inc., King & Spalding LLP, Medtronic, NeoForce Group, Philips Healthcare, PhotoMedex, Product Safety Consulting, Inc., Spine Smith, St. Jude Medical Neuromodulation, Stryker Corporation and Synthes

Article adapted by Medical News Today from original press release. Click 'references' tab above for source.
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About the Organizer
Q1 Productions designs and develops webinars, training courses, conference programs and forums aimed at specifically targeted audiences in order to provide strategic and timely information. Through a rigid production process focused on end-user research and design, our team is able to understand the immediate business concerns of today’s leading executives. Whether focusing on new or pending legislative issues, enhanced business processes or technologies that will drive efficiency and customer service, our programs provide solutions to the urgent needs of our attendees. Visit http://www.q1productions.com
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MLA

Q1 Productions designs. "Medical Device Safety Conference: Regulations, Reporting & Tracking, 27-28 August 2012, Baltimore, MD." Medical News Today. MediLexicon, Intl., 18 Jul. 2012. Web.
18 Jul. 2012. <http://www.medicalnewstoday.com/releases/247958.php>


APA
Q1 Productions designs. (2012, July 18). "Medical Device Safety Conference: Regulations, Reporting & Tracking, 27-28 August 2012, Baltimore, MD." Medical News Today. Retrieved from
http://www.medicalnewstoday.com/releases/247958.php.

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