{"id":62493,"date":"2026-01-14T16:06:13","date_gmt":"2026-01-14T15:06:13","guid":{"rendered":"https:\/\/pharma-trend.com\/en\/auditing-and-qualifying-suppliers-and-vendors-an-effective-risk-based-approach-training-course-mar-3rd-mar-5th-2026-researchandmarkets-com\/"},"modified":"2026-01-14T16:06:13","modified_gmt":"2026-01-14T15:06:13","slug":"auditing-and-qualifying-suppliers-and-vendors-an-effective-risk-based-approach-training-course-mar-3rd-mar-5th-2026-researchandmarkets-com","status":"publish","type":"post","link":"https:\/\/pharma-trend.com\/en\/auditing-and-qualifying-suppliers-and-vendors-an-effective-risk-based-approach-training-course-mar-3rd-mar-5th-2026-researchandmarkets-com\/","title":{"rendered":"Auditing and Qualifying Suppliers and Vendors: An Effective Risk-based Approach Training Course (Mar 3rd &#8211; Mar 5th, 2026) &#8211; ResearchAndMarkets.com"},"content":{"rendered":"<div>\n<p>DUBLIN&#8211;(BUSINESS WIRE)&#8211;The <a target=\"_blank\" href=\"https:\/\/www.researchandmarkets.com\/reports\/6050981\/auditing-qualifying-suppliers-vendors-effective?utm_source=BW&amp;utm_medium=PressRelease&amp;utm_code=wdcrqs&amp;utm_campaign=2132806+-+Auditing+and+Qualifying+Suppliers+and+Vendors%3A+An+Effective+Risk-based+Approach+Training+Course+(Mar+3rd+-+Mar+5th%2C+2026)&amp;utm_exec=chdomspi\" rel=\"nofollow\" shape=\"rect\">&#8220;Auditing and Qualifying Suppliers and Vendors: An Effective Risk-based Approach (Mar 3rd &#8211; Mar 5th, 2026)&#8221;<\/a> training has been added to <strong>ResearchAndMarkets.com&#8217;s<\/strong> offering.<\/p>\n<p><a href=\"https:\/\/mms.businesswire.com\/media\/20260114190950\/en\/2692064\/4\/logo.jpg\"><img decoding=\"async\" src=\"https:\/\/mms.businesswire.com\/media\/20260114190950\/en\/2692064\/22\/logo.jpg\"><\/a><br \/><a href=\"https:\/\/mms.businesswire.com\/media\/20260114190950\/en\/2692064\/4\/logo.jpg\"><img decoding=\"async\" src=\"https:\/\/mms.businesswire.com\/media\/20260114190950\/en\/2692064\/21\/logo.jpg\"><\/a><\/p>\n<p>\nSupplier or vendor qualification is a crucial component in compliance to 21 CFR 111. The FDA requires that manufacturers of <strong>dietary supplements, Pharmaceuticals, Biotech and Medical Device<\/strong> must &#8220;qualify&#8221; each of their vendors but do not provide guidance on how a company is to perform this qualification. Supplier qualification principles also apply to subcontracted services affecting cGMP (manufacturingsteps, packaging and labeling, testing and\/or calibration services, storage and distribution, etc.) Any supplier qualification program must include two critical components:<\/p>\n<ul>\n<li>\nClearly defined specifications\/requirements for all of these goods or services being purchased, and;<\/li>\n<li>\nObjective evidence to show that your requirements are being consistently fulfilled.<\/li>\n<\/ul>\n<p>\nIt is designed for those who already have a basic understanding of dietary supplement GMPs and the knowledge and skills necessary to qualify suppliers.<\/p>\n<p>\nSince the evaluation of all types of suppliers often involves auditing, this course will incorporate a fresh look at the auditing process and the skills and techniques needed to get the most from these activities. The skills and techniques learned are independent of the type of auditing or the standard being audited and will be useful when conducting internal audits and performing audits of suppliers.<\/p>\n<p>\n<strong>Why Should You Attend<\/strong><\/p>\n<p>\nThe various regulatory agencies have expectations that suppliers and vendors will demonstrate control over their manufacturing processes, validations, and documentation. Quality auditing is the process of checking whether these organizations have implemented what they have stated in written procedures and whether their people are doing what the organizations procedures state they will do.<\/p>\n<p>\n<strong>Learning Objectives<\/strong><\/p>\n<p>\nOn conclusion of this course, you will have an understanding of the following:<\/p>\n<ul>\n<li>\nRegulations that apply to vendor qualification (21 CFR 111)<\/li>\n<li>\nFood Safety Modernization Act (FSMA)<\/li>\n<li>\nImpact of FSMA on Supplier Qualification<\/li>\n<li>\nRisk assessment and risk management<\/li>\n<li>\nSupplier monitoring activities<\/li>\n<li>\nOn-site audit strategies and requirements<\/li>\n<li>\nManaging the audit process effectively before, during and after<\/li>\n<li>\nThe consequences of non-compliance<\/li>\n<\/ul>\n<p>\n<strong>This live training Seminar includes the following for each registered attendee:<\/strong><\/p>\n<ul>\n<li>\nA copy of the presentation slides by download<\/li>\n<li>\nA certificate of participation for attendee training records<\/li>\n<li>\nQ\/A Session<\/li>\n<li>\nFree Handouts on FDA Inspection<\/li>\n<\/ul>\n<p>\n<strong>Who Should Attend:<\/strong><\/p>\n<p>\nThis intensive, practical course will be of value to those professionals in the pharmaceutical, medical device and related industries who are responsible for or involved in any interaction with suppliers, including those working in:<\/p>\n<ul>\n<li>\nManagement<\/li>\n<li>\nLaboratories<\/li>\n<li>\nAuditing<\/li>\n<li>\nPurchasing<\/li>\n<li>\nQA\/QC<\/li>\n<li>\nProcurement<\/li>\n<li>\nR&amp;D<\/li>\n<li>\nLegal<\/li>\n<li>\nManufacturing<\/li>\n<li>\nValidation<\/li>\n<li>\nRegulatory Affairs<\/li>\n<li>\nDocumentation Management<\/li>\n<\/ul>\n<p>\n<strong>Key Topics Covered:<\/strong><\/p>\n<p>\n<strong>Topic 1: The Benefits of Effective Supplier Management<\/strong><\/p>\n<ul>\n<li>\nKey Components of a Supplier Management Program<\/li>\n<\/ul>\n<p>\n<strong>Topic 2: Regulatory Guidance Review<\/strong><\/p>\n<ul>\n<li>\nUnderstanding Regulatory Requirements and Standards for Supplier and Contract<\/li>\n<li>\nManufacturer (CM) Management:<\/p>\n<ul>\n<li>\nUnited States Food and Drug Association (FDA) regulations and guidance<\/li>\n<li>\nEuropean Union (EU) directives and guidelines<\/li>\n<li>\nInternational Standardization Association (ISO) standards<\/li>\n<li>\nExamples of regulatory findings<\/li>\n<\/ul>\n<\/li>\n<\/ul>\n<p>\n<strong>Topic 3: The Cost of Poor Quality from Suppliers and CMs:<\/strong><\/p>\n<ul>\n<li>\nHow to speak management&#8217;s language<\/li>\n<\/ul>\n<p>\n<strong>Topic 4: Strategic Management of Suppliers:<\/strong><\/p>\n<ul>\n<li>\nDeveloping a strategic plan based on your company and environment<\/li>\n<li>\nRisk Management &#8211; A Lifecycle Approach:<\/li>\n<li>\nTemplate for a risk assessment<\/li>\n<\/ul>\n<p>\n<strong>Topic 5: Supplier qualification<\/strong><\/p>\n<ul>\n<li>\nSelecting a Supplier or Contract Manufacturer<\/li>\n<li>\nObtaining information on suppliers<\/li>\n<li>\nTools for making the selection<\/p>\n<ul>\n<li>\nSupplier Assessments:<\/li>\n<li>\nDesktop assessments<\/li>\n<li>\nSupplier audits<\/li>\n<li>\nHandling Supplier Transitions<\/li>\n<\/ul>\n<\/li>\n<li>\nHow to use your strategic plan to make decisions<\/li>\n<li>\nWhen to use a sole source supplier<\/li>\n<li>\nBuilding a Relationships with a Supplier or Contract Manufacturer<\/li>\n<li>\nMaking your Supplier Quality Agreement a Great Resource:<\/p>\n<ul>\n<li>\nQuality Agreement Template<\/li>\n<\/ul>\n<\/li>\n<li>\nMonitoring Your Supplier&#8217;s Performance to Reduce Risks and Costs:<\/p>\n<ul>\n<li>\nTemplate for a supplier scorecard<\/li>\n<\/ul>\n<\/li>\n<li>\nManaging nonconforming events<\/li>\n<li>\nPartnering with a Supplier or CM for Improvement:<\/p>\n<ul>\n<li>\nTools for improvement<\/li>\n<\/ul>\n<\/li>\n<\/ul>\n<p>\n<strong>Speakers:<\/strong><\/p>\n<p>\nKelly Thomas<br \/>\n<br \/>Vice President<br \/>\n<br \/>Stallergenes Greer<\/p>\n<p>\nMs. Thomas has over two decades of cGMP hands-on industry experience in both pharmaceutical and medical device manufacturing operations. Her experience covers all Quality Systems; as well as, all areas of validation; including, process\/product validation, facilities validation, CSV and 21 CFR Part 11, test method validation, equipment\/automated processes and cleaning validation.<\/p>\n<p>\nUtilizing strategic thinking, risk based approaches, and Lean principles, she has demonstrated success in steering and managing complex projects within the pharmaceutical and medical device industries.<\/p>\n<p>\nFor more information about this training visit <a target=\"_blank\" href=\"https:\/\/www.researchandmarkets.com\/reports\/6050981\/auditing-qualifying-suppliers-vendors-effective?utm_source=BW&amp;utm_medium=PressRelease&amp;utm_code=wdcrqs&amp;utm_campaign=2132806+-+Auditing+and+Qualifying+Suppliers+and+Vendors%3A+An+Effective+Risk-based+Approach+Training+Course+(Mar+3rd+-+Mar+5th%2C+2026)&amp;utm_exec=chdomspi\" rel=\"nofollow\" shape=\"rect\">https:\/\/www.researchandmarkets.com\/r\/hiyueq<\/a><\/p>\n<p>\n<strong>About ResearchAndMarkets.com<\/strong><\/p>\n<p>\nResearchAndMarkets.com is the world&#8217;s leading source for international market research reports and market data. We provide you with the latest data on international and regional markets, key industries, the top companies, new products and the latest trends.<\/p>\n<p> <b>Contacts<\/b> <\/p>\n<p>\nResearchAndMarkets.com<br \/>\n<br \/>Laura Wood, Senior Press Manager<br \/>\n<br \/><a target=\"_blank\" href=\"&#109;&#97;&#x69;l&#116;&#x6f;&#x3a;p&#114;&#x65;&#x73;s&#64;&#x72;e&#115;&#x65;&#x61;r&#99;&#x68;&#x61;n&#100;&#x6d;a&#114;&#x6b;&#x65;t&#115;&#x2e;&#x63;o&#109;\" rel=\"nofollow\" shape=\"rect\">&#x70;&#114;e&#x73;&#x73;&#64;r&#x65;&#x73;&#101;a&#x72;&#x63;&#104;a&#x6e;&#x64;&#109;a&#x72;&#107;&#101;t&#x73;&#46;c&#x6f;&#x6d;<\/a><\/p>\n<p>For E.S.T Office Hours Call 1-917-300-0470<br \/>\n<br \/>For U.S.\/ CAN Toll Free Call 1-800-526-8630<br \/>\n<br \/>For GMT Office Hours Call +353-1-416-8900<\/p>\n<\/div>\n","protected":false},"excerpt":{"rendered":"<p>DUBLIN&#8211;(BUSINESS WIRE)&#8211;The &#8220;Auditing and Qualifying Suppliers and Vendors: An Effective Risk-based Approach (Mar 3rd &#8211; Mar 5th, 2026)&#8221; training has been added to ResearchAndMarkets.com&#8217;s offering. Supplier or vendor qualification is a crucial component in compliance to 21 CFR 111. The FDA requires that manufacturers of dietary supplements, Pharmaceuticals, Biotech and Medical Device must &#8220;qualify&#8221; each &#8230; <span class=\"more\"><a class=\"more-link\" href=\"https:\/\/pharma-trend.com\/en\/auditing-and-qualifying-suppliers-and-vendors-an-effective-risk-based-approach-training-course-mar-3rd-mar-5th-2026-researchandmarkets-com\/\">[Read more&#8230;]<\/a><\/span><\/p>\n","protected":false},"author":4,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[13],"tags":[],"class_list":{"0":"entry","1":"post","2":"publish","3":"author-business","4":"post-62493","6":"format-standard","7":"category-industry"},"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.4 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Auditing and Qualifying Suppliers and Vendors: An Effective Risk-based Approach Training Course (Mar 3rd - Mar 5th, 2026) - ResearchAndMarkets.com - Pharma Trend<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/pharma-trend.com\/en\/auditing-and-qualifying-suppliers-and-vendors-an-effective-risk-based-approach-training-course-mar-3rd-mar-5th-2026-researchandmarkets-com\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Auditing and Qualifying Suppliers and Vendors: An Effective Risk-based Approach Training Course (Mar 3rd - Mar 5th, 2026) - ResearchAndMarkets.com - Pharma Trend\" \/>\n<meta property=\"og:description\" content=\"DUBLIN&#8211;(BUSINESS WIRE)&#8211;The &#8220;Auditing and Qualifying Suppliers and Vendors: An Effective Risk-based Approach (Mar 3rd &#8211; Mar 5th, 2026)&#8221; training has been added to ResearchAndMarkets.com&#8217;s offering. 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Supplier or vendor qualification is a crucial component in compliance to 21 CFR 111. The FDA requires that manufacturers of dietary supplements, Pharmaceuticals, Biotech and Medical Device must &#8220;qualify&#8221; each ... 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