{"product_id":"2940011837326","title":"Current Good Manufacturing Practices: Pharmaceutical, Biologics, and Medical Device Regulations and Guidance Documents Concise Reference","description":"FDA Regulations and Associated Guidance Documents:  -  Part 11 Electronic Records; Electronic Signatures  -  Part 26  Mutual Recognition of Pharmaceutical Good Manufacturing Practice Reports, Medical Device Quality System Audit Reports, and Certain Medical Device Product Evaluation Reports: United States and the European Community  -  Part 200  Drugs General  -  Part 207  Registration of Producers of Drugs and Listing of Drugs in Commercial Distribution  -  Part 210  Current Good Manufacturing Practice in Manufacturing, Processing, Packing, or Holding of Drugs  -  Part 211  Current Good Manufacturing Practice For Finished Pharmaceuticals  -  Part 600  Biological Products: General  -  Part 807  Establishment Registration and Device Listing for Manufacturers and Initial Importers of Devices  -  Part 820  Quality System Regulation    Reference Tools:    -  Glossaries combined in one location  -  GMP Keyword Index for 21CFR211  -  Combined Index for all documents","brand":"PharmaLogika","offers":[{"title":"Default Title","offer_id":47173990449392,"sku":"2940011837326","price":42.99,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0737\/7593\/9824\/files\/2940011837326_p0.jpg?v=1763550529","url":"https:\/\/shop-qa.barnesandnoble.com\/products\/2940011837326","provider":"Barnes \u0026 Noble (DEV)","version":"1.0","type":"link"}