Wondering what would improve your device company’s CAPA performance? We have answers from an exclusive, new FDAnews survey of devicemakers:
These findings are part of an FDAnews survey of medical device manufacturers that will take you inside your colleagues’ quality departments to understand how they are approaching the industry’s CAPA headaches.
For the first time ever, FDAnews surveyed 229 medical devicemakers to reveal how the industry is approaching CAPA investigations, what the industry is experiencing in terms of enforcement, and what best practices exist to better manage CAPA investigations.
Buy now to get an unprecedented look inside CAPA programs throughout the industry as well as benchmarks and insights to help you structure your CAPA system for maximum effectiveness and justify your positions with upper management.
In this timely, easy-to-read report, FDAnews pulls back the curtain on CAPA investigations to give you actionable intelligence on questions such as:
Complete with 34 tables and analysis, this report will help devicemakers uncover and correct the attitudes and procedures that undermine product quality and leave them vulnerable to recalls, product failures and FDA violations. Discover innovative new techniques for taming CAPA system problems, improving your performance and driving change in your organization.
Medical Device Manufacturer CAPA Benchmarking Survey is offered by FDAnews in print or PDF format for $457.
There's no risk when you purchase from FDAnews with our money-back guarantee. Not satisfied with your publication? Return the hard copy within 30 days (in resalable condition), and we will refund 100 percent of your purchase price (less shipping/handling). For the PDF version, you must notify FDAnews within 24 hours of receipt of purchase to receive a refund.
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