{"product_id":"21-cfr-parts-11-820-qsr-with-updated-2026-qmsr","title":"21 CFR Parts 11, 820 QSR with Updated 2026 QMSR","description":"\u003ch3\u003e\u003cstrong\u003e21 CFR Parts 11 Electronic Records, 820 Quality System Regulation and 2026 Updated Quality Management System Regulation (2-February 2024 Update)\u003c\/strong\u003e\u003c\/h3\u003e\n\u003cp\u003e\u003cstrong\u003e21 CFR Part 11 with Scope and Application 2003\u003c\/strong\u003e\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003e21 CFR Part 820 Quality System Regulation \u003c\/strong\u003e\u003c\/p\u003e\n\u003cp\u003eCurrent good manufacturing practice (CGMP) requirements are set forth in this quality system regulation. The requirements in this part govern the methods used in, and the facilities and controls used for, the design, manufacture, packaging, labeling, storage, installation, and servicing of all finished devices intended for human use.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003ePART 820 -- QUALITY MANAGEMENT SYSTEM REGULATION\u003c\/strong\u003e\u003cbr\u003e\u003cstrong\u003eSUMMARY:\u003c\/strong\u003e The FDA is issuing a final rule to amend the device current good manufacturing practice (CGMP) requirements of the Quality System (QS) regulation to harmonize and modernize the regulation.\u003c\/p\u003e\n\u003cp\u003e- - - - - - - - - - - - - - - - - - - - -\u003c\/p\u003e\n\u003cp\u003e\u003cbr\u003e\u003c\/p\u003e","brand":"GMP Publications","offers":[{"title":"Default Title","offer_id":47304209694955,"sku":null,"price":5.95,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0790\/1498\/5963\/files\/21CFR11-820QSR-820QMSR-C-260401_8962a0f8-ac9d-4fbd-8d17-c5703489ea7c.png?v=1773744485","url":"https:\/\/gmppublications.com\/products\/21-cfr-parts-11-820-qsr-with-updated-2026-qmsr","provider":"GMP","version":"1.0","type":"link"}