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The product is a trade paperback book titled "21 CFR-Parts 820 Quality System Regulation: Code of Federal Regulations - FDA" published by the GMP Institute in 1997. It is a regulation book focused on current good manufacturing practices for medical devices and in vitro diagnostic products. With 46 pages, this book covers the quality system regulation needed for compliance with FDA regulations. Written in English, it serves as a valuable resource for those in need of understanding and following the guidelines for medical device and in vitro diagnostic product manufacturing.
When you click on links to various merchants on this site and make a purchase, this can result in this site earning a commission. Affiliate programs and affiliations include, but are not limited to, the eBay Partner Network.