Enhanced Software Eases FDA Compliance
Fri, 12/05/2008 - 7:04am
An upgrade to the Magellon Quality Lifecycle Management (QLM) software gives medical device-makers a streamlined way to rapidly deliver quality products and maintain compliance with the FDA's Title 21 CFR Part 11. The solution brings together the data, analysis, and processes required to bring high-quality products to market quickly and efficiently. Magellon now includes electronic device history record data capture and storage to trace key product test, quality, and manufacturing process records electronically, from design through manufacturing and post-sales support.