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Each attendee will be logged into the Webinar with their own unique email address for accountability and all Attendees must satisfy 7 hours of 'eye's on' training to get a certificate of attendance. A GMP Publications representative will contact the purchaser for the email address(es) of each attendee who purchases a Desk Reference Set.  Go to \u003ca title=\"GMP Boot Camps\" href=\"https:\/\/www.gmpbootcamps.com\" rel=\"noopener\" target=\"_blank\"\u003ehttps:\/\/www.gmpbootcamps.com\u003c\/a\u003e for Course description.\u003c\/p\u003e","brand":"GMP Publications","offers":[{"title":"Default Title","offer_id":46993535205611,"sku":null,"price":49.95,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0790\/1498\/5963\/files\/DeskReference.jpg?v=1763740157"},{"product_id":"deacontrolledsubstancesgmp-htm","title":"FDA DEA GMP Master Reference Guide","description":"\u003cp\u003e\u003cspan\u003e\u003cstrong\u003e\u003cu\u003eUS FDA Title 21 CFR\u003c\/u\u003e\u003c\/strong\u003e\u003c\/span\u003e\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003ePart 11 - Electronic Records; Electronic Signatures\u003c\/li\u003e\n\u003cli\u003ePart 11 - Electronic Records; 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Electronic Signatures,\u003c\/li\u003e\n\u003cli\u003e21 CFR Part 11 - Scope \u0026amp; Application 2003\u003c\/li\u003e\n\u003cli\u003e21 CFR Parts 210\/211, Drug GMPs,\u003c\/li\u003e\n\u003cli\u003e21 CFR Parts 600, General Biologic,\u003c\/li\u003e\n\u003cli\u003e21 CFR Parts 601 Licensing, \u003c\/li\u003e\n\u003cli\u003e21 CFR Parts 610 Biologic GMPs\u003c\/li\u003e\n\u003cli\u003e21 CFR Part 820 - Quality Management System Regulations (QMSR) 2026\u003c\/li\u003e\n\u003cli\u003eGMPs for Phase 1 Investigational Drugs, July 2008\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003cspan style=\"text-decoration: underline;\"\u003e\u003cstrong\u003eInternational GMPs and Guidance:\u003c\/strong\u003e\u003c\/span\u003e\u003c\/p\u003e\n\u003cp\u003e• EU EudraLex - Volume 4 - Good Manufacturing Practice (GMP)\u003cbr\u003e   - Chapter 1 - Pharmaceutical Quality System\u003cbr\u003e   - Chapter 2 - Personnel\u003cbr\u003e   - Chapter 3 - Premise and Equipment\u003cbr\u003e   - Chapter 4 - Documentation\u003cbr\u003e   - Chapter 5 - Production\u003cbr\u003e   - Chapter 6 - Quality Control\u003cbr\u003e   - Chapter 7 - Outsourced activities\u003cbr\u003e   - Chapter 8 - Complaints and Product Recall\u003cbr\u003e   - Chapter 9 - Self Inspection\u003cbr\u003e• 2023 Annex 1 Manufacture of Sterile Medicinal Products\u003cbr\u003e• ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients\u003c\/p\u003e\n\u003cp\u003e- - - - - - - - - - - - - - - - - - - - - - - - - - \u003c\/p\u003e","brand":"GMP Publications","offers":[{"title":"Default Title","offer_id":46993536811243,"sku":"978-1-935131-81-6","price":17.95,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0790\/1498\/5963\/files\/GMPManufHandbook.png?v=1773859292"},{"product_id":"eu-cgmps-for-atmp-2018-guidelines-on-good-manufacturing-practice-specific-to-advanced-therapy-medicinal-products","title":"EU cGMPs for ATMP - 2018 Advanced Therapy Medicinal Products","description":"\u003cp\u003e\u003cstrong\u003eEudraLex\u003c\/strong\u003e\u003cbr\u003e\u003cstrong\u003eThe Rules Governing Medicinal Products \u003c\/strong\u003e\u003cstrong\u003ein the European Union\u003c\/strong\u003e\u003cbr\u003e\u003cstrong\u003eVolume 4\u003c\/strong\u003e\u003cbr\u003e\u003cstrong\u003eGood Manufacturing Practice\u003c\/strong\u003e\u003cbr\u003e\u003cstrong\u003eGuidelines on Good Manufacturing Practice \u003c\/strong\u003e\u003cstrong\u003especific to Advanced Therapy Medicinal Products\u003c\/strong\u003e\u003c\/p\u003e\n\u003cp\u003eIn Operation: 22 May 2018\u003c\/p\u003e\n\u003cp\u003eAdvanced therapy medicinal products that are administered to patients under Article 3(7) of Directive 2001\/83\/EC1 (so called “hospital exemption”) must be manufactured under equivalent quality standards to the manufacturing of advanced therapy medicinal products with a marketing authorisation.\u003c\/p\u003e","brand":"GMP Publications","offers":[{"title":"Default Title","offer_id":46993536876779,"sku":null,"price":6.95,"currency_code":"USD","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0790\/1498\/5963\/files\/ATMP.jpg?v=1763427141"},{"product_id":"gmp-boot-camp-certificate-and-gmp-handbook-details-html","title":"8-Hour Monthly GMP Training, Certificate, GMP Handbook \u0026 e-Workbook","description":"\u003cp\u003e\u003cbr\u003e\u003c\/p\u003e\n\u003ctable style=\"height: 971px; width: 550px;\" border=\"1\" width=\"550\" cellspacing=\"2\" cellpadding=\"2\"\u003e\n\u003ctbody\u003e\n\u003ctr style=\"height: 971px;\"\u003e\n\u003ctd style=\"width: 600px; height: 971px;\" align=\"left\" valign=\"top\"\u003e\n\u003ctable style=\"width: 550px; border-collapse: collapse;\" border=\"1\"\u003e\n\u003ctbody\u003e\n\u003ctr\u003e\n\u003ctd style=\"width: 100%;\" align=\"left\" valign=\"middle\" bgcolor=\"#E2EBFF\" height=\"60\"\u003e\n\u003ch2\u003e\u003cstrong\u003eMonthly GMP Training includes Registration Fee, and...\u003c\/strong\u003e\u003c\/h2\u003e\n\u003cp\u003e\u003cstrong\u003eCheck dates at www.gmpbootcamps.com\u003c\/strong\u003e\u003c\/p\u003e\n\u003cul\u003e\n\u003cli\u003e\n\u003cdiv\u003e8 Hour Live GMP QMS \u0026amp; 21 CFR Part 11 Training Hosted by:\u003c\/div\u003e\n\u003cul\u003e\n\u003cli\u003eGMP Boot Camps and\u003c\/li\u003e\n\u003cli\u003eGMP Publications\u003c\/li\u003e\n\u003cli\u003eThe Auditing Group\u003cbr\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003c\/li\u003e\n\u003cli\u003eCertificate of Attendance**\u003cbr\u003e\n\u003c\/li\u003e\n\u003cli\u003eStandard GMP Handbook, US FDA 21 CFR Parts 11, 210\/211 \u0026amp; 820 Pocket Guide.\u003cbr\u003e\n\u003c\/li\u003e\n\u003cli\u003ee-Workbook - Over 300+ Slides on a Note Style e-Workbook.\u003c\/li\u003e\n\u003cli\u003eFree Registration for 1-year annual training date\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003eNOTE: Each person must register with a unique email address to get credit. \u003cbr\u003efor more information go to \u003ca title=\"GMP Boot Camp website\" href=\"https:\/\/www.gmpbootcamps.com\" rel=\"noopener\" target=\"_blank\"\u003eGMP Boot Camp website Terms\u003c\/a\u003e. \u003cspan style=\"font-size: 0.875rem;\"\u003e See \u003c\/span\u003e\u003ca href=\"http:\/\/www.gmpbootcamps.com\" style=\"font-size: 0.875rem;\"\u003ewww.gmpbootcamps.com\u003c\/a\u003e\u003cspan style=\"font-size: 0.875rem;\"\u003e for Free GMP QMS Training Schedule.\u003c\/span\u003e\u003c\/p\u003e\n\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr\u003e\n\u003ctd style=\"width: 100%; text-align: center;\" bgcolor=\"#E2EBFF\"\u003e\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003c\/tbody\u003e\n\u003c\/table\u003e\n\u003cbr\u003e\n\u003ctable style=\"height: 926px; width: 550px;\" border=\"0\" width=\"550\" cellspacing=\"2\" cellpadding=\"2\"\u003e\n\u003ctbody\u003e\n\u003ctr style=\"height: 445px;\"\u003e\n\u003ctd style=\"width: 265px; height: 54px;\" align=\"left\" valign=\"top\"\u003e\u003cimg alt=\"\" src=\"https:\/\/cdn.shopify.com\/s\/files\/1\/0790\/1498\/5963\/files\/10Part11210211820ICHq7-1.jpg?v=1763228155\"\u003e\u003c\/td\u003e\n\u003ctd style=\"width: 250.719px; height: 54px;\" align=\"left\" valign=\"top\"\u003e\n\u003cp\u003e\u003cstrong\u003eUS FDA Title 21 CFR Part 11 Electronic Records; Electronic Signatures\u003c\/strong\u003e with Scope and Application 2003 - FDA Interpretation of Part 11.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eUS FDA Title 21 CFR Parts 210\/211 Good Manufacturing Practices\u003c\/strong\u003e - The regulations containing the minimum CGMPs for methods, facilities or controls to be used for manufacture, processing, packing, or holding of a drug product.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eUS FDA Title 21 CFR Part 820 Quality Systems Regulation\u003c\/strong\u003e The controls used for, the design, manufacture, packaging, labeling, storage, installation, and servicing of all finished devices.\u003c\/p\u003e\n\u003cp\u003e\u003cstrong\u003eICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients.\u003c\/strong\u003e  The ICH Guidance supporting APIs for manufacturing of Drug Substance for Finished Products.\u003c\/p\u003e\n\u003c\/td\u003e\n\u003c\/tr\u003e\n\u003ctr style=\"height: 18px;\"\u003e\n\u003ctd style=\"height: 18px; 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