Design Control for Medical Devices
Meeting FDAâ€™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 â€“ 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, thereâ€™s relentless pressure from both FDA and Congress to improve device design control and manufacturing.