FDAnews Announces New Conference: Medical Device Compliance Institute, May 13-16, 2014

To survive in today's tough economy and ultra-competitive medical device market, manufacturers need a quality system that works from the get-go. Medical Device Quality & Compliance Institute 2014: Quality Systems and Design Control Training is three-and-a-half days of intensive training on compliance guidance and insight needed to meet FDA standards with confidence.

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Medical Device Quality Compliance Institute

Medical Device Quality Compliance Institute

Falls Church, VA (PRWEB) March 21, 2014

Medical Device Quality & Compliance Institute 2014:
Quality Systems and Design Control Training
May 13-16, 2014 – Frederick, MD
http://www.fdanews.com/MDCI
The FDA says approximately 44% of device recalls are due to faulty design.

Recalls are expensive, embarrassing and often lead to more serious financial consequences, not only from the FDA but also from courts and unhappy shareholders.

To survive in today's tough economy and ultra-competitive medical device market, manufacturers need a quality system that works from the get-go, from the start of product design, continuing through component selection, manufacturing, use and disposal.

Register now for Medical Device Quality & Compliance Institute 2014: Quality Systems and Design Control Training, two courses presented by EduQuest in cooperation with FDAnews that are offered separately or as an integrated three-and-a-half-day learning package, and learn how to develop a by-the-book quality management program. Leave the guessing to the competition.

Discover how to overcome one of the biggest obstacles device manufacturers face, how the FDA expects manufacturers to develop and implement design controls, then transfer product design to manufacturing operations.

With three-and-a-half days of intensive training attendees will walk away with the compliance guidance and insight needed to meet FDA standards with confidence.

Learn straight from the source, former FDA inspectors, rulemakers and trainers from the global consulting team of EduQuest, headquartered near Washington, DC. The instructors include one of the co-authors and trainers of the FDA's Quality System Inspection Technique (QSIT) and the founding editor and co-author of the FDA's "bible" for inspectors, the Investigations Operations Manual (IOM).

Through plain-English instruction, detailed course materials and interactive exercises that reinforce the lessons (not to mention make the classroom more fun and interesting), attendees will learn to cost-effectively comply with the FDA's QSR rules and related international standards.

Specifically targeted to device manufacturers and suppliers, the institute gives a thorough understanding of the massive 21 CFR 820 Quality Systems Regulation requirements. Know what it takes to stay in compliance and avoid the risk of a product not getting to market or being removed from the market once it's there.

Conference Details:
Medical Device Quality & Compliance Institute 2014:
Quality Systems and Design Control Training
May 13-16, 2014 – Frederick, MD
http://www.fdanews.com/MDCI

Tuition: $2,997

Easy Ways to Register:
Online: http://www.fdanews.com/MDCI
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.

About EduQuest:
Since its founding in 1995, EduQuest has trained staff in the FDA Office of Regulatory Affairs (ORA), which is responsible for FDA field inspections and product recalls. In addition, EduQuest has trained and advised industry professionals worldwide. Martin Browning, the president of EduQuest and primary developer of EduQuest training classes, co-wrote the FDA Part 11 rule for electronic records and electronic signatures during his 22 years at FDA.


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