March 18-19, 2010 – Design Control for Medical Devices

Design Control for Medical Devices

Meeting FDA’s 21 CFR 820.30 Rules for Quality Design and Manufacturing

2 day course (8:30 a.m. – 5:30 p.m.)

Get Your Training Direct from Former FDA Device Officials

Learn straight from the source – former FDA inspectors, rulemakers, and trainers from the global consulting team of EduQuest.

• March 18-19, 2010, Las Vegas, NV
• September 21-22, 2010, Wilmington, DE

Design control is required for all medical devices sold in the U.S., EU, Japan, and several other countries. In addition, there’s relentless pressure from both FDA and Congress to improve device design control and manufacturing.

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