{"id":53050,"date":"2023-01-18T18:02:46","date_gmt":"2023-01-18T17:02:46","guid":{"rendered":"https:\/\/pharma-trend.com\/en\/2-day-seminar-quality-and-gmp-compliance-for-virtual-companies-pharmaceutical-and-biologics-industries-march-2-3-2023-researchandmarkets-com\/"},"modified":"2023-01-18T18:02:46","modified_gmt":"2023-01-18T17:02:46","slug":"2-day-seminar-quality-and-gmp-compliance-for-virtual-companies-pharmaceutical-and-biologics-industries-march-2-3-2023-researchandmarkets-com","status":"publish","type":"post","link":"https:\/\/pharma-trend.com\/en\/2-day-seminar-quality-and-gmp-compliance-for-virtual-companies-pharmaceutical-and-biologics-industries-march-2-3-2023-researchandmarkets-com\/","title":{"rendered":"2 Day Seminar Quality and GMP Compliance for Virtual Companies (Pharmaceutical and Biologics Industries) (March 2-3, 2023) &#8211; ResearchAndMarkets.com"},"content":{"rendered":"<div>\n<p>DUBLIN&#8211;(BUSINESS WIRE)&#8211;The <a target=\"_blank\" href=\"https:\/\/www.researchandmarkets.com\/reports\/5714341\/2-day-seminar-quality-and-gmp-compliance-for?utm_source=BW&amp;utm_medium=PressRelease&amp;utm_code=4cq3b8&amp;utm_campaign=1809638+-+2+Day+Seminar+Quality+and+GMP+Compliance+for+Virtual+Companies+(Pharmaceutical+and+Biologics+Industries)+(March+2-3%2C+2023)&amp;utm_exec=como322prd\" rel=\"nofollow noopener\" shape=\"rect\">&#8220;2 Day Seminar Quality and GMP Compliance for Virtual Companies (Pharmaceutical and Biologics Industries)&#8221;<\/a> training has been added to <strong>ResearchAndMarkets.com&#8217;s<\/strong> offering.\n<\/p>\n<p><a href=\"https:\/\/mms.businesswire.com\/media\/20230118005782\/en\/1689494\/4\/logo.jpg\"><img decoding=\"async\" src=\"https:\/\/mms.businesswire.com\/media\/20230118005782\/en\/1689494\/21\/logo.jpg\"><\/a><\/p>\n<p>\nToday, many companies operate on an outsourcing model. This is very common for companies who are evolving from being mainly development-focused to a point where they are entering latter stages of Phase 2 or Phase 3 clinical trials, and plan to have a product ready for market approval in the coming months. Most such companies are small, and may not have deep expertise in QA and GMP compliance, relying on their partners to cover those areas. Companies who outsource the majority of operations through the use of Contract Manufacturing Organizations (CMOs), Contract Research Organizations (CROs) and Contract Laboratories, however, remain responsible for the quality and compliance status of the products they send to the clinic or to the marketplace.\n<\/p>\n<p>\nIn this two day workshop conference you will learn the requirements and expectations of major health care regulators that are applicable to &#8220;virtual&#8221; companies. You will learn how to diagnose your company&#8217;s needs based on which GMP and GCP-governed operations you retain and which you outsource; what the current expectations and best industry practices are for selecting, qualifying and monitoring your contractors to ensure they are meeting your requirements; and how to build a quality system framework that is not excessive for your current needs, but has the structure and integration to &#8220;grow with you&#8221; as the scope your operations change in the coming months and years.\n<\/p>\n<p>\nYou will also learn best practices for managing a regulatory inspection, with emphasis on FDA, EMA and Health Canada, but applicable to most other major agencies as well.\n<\/p>\n<p>\n<strong>Learning Objectives:<\/strong>\n<\/p>\n<p>\nParticipants in this seminar will:\n<\/p>\n<ul>\n<li>\nUnderstand the GMP and GCP requirements all virtual companies must meet regardless of the extent of their outsourcing operations\n<\/li>\n<li>\nUnderstand how to select, qualify and monitor CMOs, CROs and Contract Laboratories\n<\/li>\n<li>\nLearn the elements to include in a quality agreement (also known as a technical agreement)\n<\/li>\n<li>\nLearn how to determine which GMP or GCP requirements apply to you, depending on the things you do internally and those you outsource\n<\/li>\n<li>\nUnderstand your obligations under the law for products you release to the clinic or the marketplace\n<\/li>\n<li>\nAppreciate the importance of maintaining data integrity\n<\/li>\n<li>\nLearn how to effectively manage a health regulatory inspection:\n<\/li>\n<li>\nInspection logistics\n<\/li>\n<li>\nResponding effectively to document requests and questions from inspectors\n<\/li>\n<li>\nManaging the inspection exit discussion\n<\/li>\n<li>\nHow to write an effective response to inspection observations\n<\/li>\n<li>\nHow to find applicable inspection references and procedures of the FDA, EMA and Health Canada\u00a0\n<\/li>\n<\/ul>\n<p>\n<strong>Who Should Attend:<\/strong>\n<\/p>\n<p>\nThis course is designed for those charged with managing Quality Assurance and Regulatory Affairs for companies in the development or commercial phase of growth who either release investigational drugs to clinical trial sites or send commercial products to the market, but rely to a great extent on the use of Contract Manufacturers and\/or Contract Laboratories.\n<\/p>\n<p>\n<strong>The following personnel will benefit from the course:<\/strong>\n<\/p>\n<ul>\n<li>\nSenior quality managers in manufacturing QA\/GMP or clinical quality areas\n<\/li>\n<li>\nQuality professionals\n<\/li>\n<li>\nRegulatory professionals\n<\/li>\n<li>\nClinical Operations\n<\/li>\n<li>\nCompliance professionals\n<\/li>\n<li>\nQuality auditors &#8211; GMP and GCP\n<\/li>\n<li>\nDocument control specialists\u00a0\n<\/li>\n<\/ul>\n<p>\n<strong>Agenda<\/strong>\n<\/p>\n<p>\n<strong>DAY 01(12:00 PM &#8211; 04:00 PM EDT)<\/strong>\n<\/p>\n<ul>\n<li>\nIntroductions and participant expectations for the program\n<\/li>\n<li>\nFundamentals of Good Manufacturing Practice<\/p>\n<ul>\n<li>\nWhat is GMP?\n<\/li>\n<li>\nPurpose of GMP\n<\/li>\n<li>\nBasis in law: US, Europe, Canada\n<\/li>\n<li>\nElements that apply to all virtual companies\n<\/li>\n<li>\nElements that depend on how operations are conducted: How to tell what applies to your company\n<\/li>\n<\/ul>\n<\/li>\n<\/ul>\n<p>\n<strong>Data Integrity: What it is and why it is important to GMP<\/strong>\n<\/p>\n<p>\n<strong>Fundamentals of Good Clinical Practice (GCP)<\/strong>\n<\/p>\n<ul>\n<li>\nWhat is GCP?\n<\/li>\n<li>\nPurpose of GCP\n<\/li>\n<li>\nBasis in law: US, Europe, Canada\n<\/li>\n<li>\nElements that apply to all virtual companies\n<\/li>\n<li>\nElements that depend on how operations are conducted: How to tell what applies to your company\n<\/li>\n<\/ul>\n<p>\n<strong>Regulatory and business risks: The case for compliance<\/strong>\n<\/p>\n<p>\n<strong>Virtual company organizational structure and responsibility for QA\/GMP\/GCP<\/strong>\n<\/p>\n<p>\n<strong>Virtual company quality system structure and management<\/strong>\n<\/p>\n<ul>\n<li>\nPolicies, procedures, documentation management\n<\/li>\n<li>\nMetrics and management review considerations\n<\/li>\n<\/ul>\n<p>\n<strong>Selection, qualification and monitoring of contractors<\/strong>\n<\/p>\n<ul>\n<li>\nInitial due diligence &#8211; public information sources to gage compliance\n<\/li>\n<li>\nQualification of vendors\n<\/li>\n<li>\nQuality agreements &#8211; determining and documenting responsibilities for GMP\n<\/li>\n<li>\nVendor audit program\n<\/li>\n<\/ul>\n<p>\n<strong>Day One Q&amp;A and recap of progress meeting stated course expectations<\/strong>\n<\/p>\n<p>\n<strong>DAY 02(12:00 PM &#8211; 04:00 PM EDT)<\/strong>\n<\/p>\n<p>\n<strong>Regulatory Inspections<\/strong>\n<\/p>\n<ul>\n<li>\nPurpose of an inspection\n<\/li>\n<li>\nReasons for inspections\n<\/li>\n<li>\nInspections at virtual company headquarters locations &#8211; purpose and scope\n<\/li>\n<li>\nInspections at CMOs and Contract Labs\n<\/li>\n<li>\nGMP inspections versus Preapproval inspections &#8211; FDA\n<\/li>\n<li>\nGCP inspections of sponsors of clinical trials\n<\/li>\n<li>\nEMA inspections &#8211; contrast with FDA\n<\/li>\n<li>\nHealth Canada inspections\n<\/li>\n<\/ul>\n<p>\n<strong>Logistics for managing inspections at your location<\/strong>\n<\/p>\n<ul>\n<li>\nInformation sources about inspections on agency websites: What you need and how to find it easily\n<\/li>\n<li>\nPreparation for inspections\n<\/li>\n<li>\nOverall process &#8211; ready room support\n<\/li>\n<li>\nReceiving and hosting the inspectors\n<\/li>\n<li>\nProviding documents\n<\/li>\n<li>\nAnswering questions\n<\/li>\n<li>\nInterpersonal dos and don&#8217;ts for interacting with inspectors\n<\/li>\n<li>\nManaging the exit discussion at the conclusion of the inspection\n<\/li>\n<\/ul>\n<p>\n<strong>Inspections at your contract organizations<\/strong>\n<\/p>\n<ul>\n<li>\nMaking sure your CMO and contract lab are &#8220;PAI ready&#8221;\n<\/li>\n<li>\nTraining employees to assure inspection readiness &#8211; pitfalls to make sure you avoid\n<\/li>\n<li>\nConducting mock inspections effectively\n<\/li>\n<\/ul>\n<p>\n<strong>Post-inspection communications with the inspecting agenc<\/strong>y\n<\/p>\n<ul>\n<li>\nHow to write an effective response\n<\/li>\n<li>\nCommon mistakes to avoid\n<\/li>\n<li>\nFollowing up to ensure the response is satisfactory\n<\/li>\n<li>\nWhen to request a meeting, and if granted, how best to handle it\n<\/li>\n<\/ul>\n<p>\n<strong>Enforcement considerations<\/strong>\n<\/p>\n<ul>\n<li>\nFDA enforcement process &#8211; domestic and ex-US\n<\/li>\n<li>\nEMA enforcement\n<\/li>\n<li>\nHealth Canada\n<\/li>\n<\/ul>\n<p>\n<strong>Final Q&amp;A, discussion, and conclusion<\/strong>\n<\/p>\n<p>\n<strong>4:00 PM: Adjourn<\/strong>\n<\/p>\n<p>\n<strong>Speakers:<\/strong>\n<\/p>\n<p>\nKelly Thomas\n<\/p>\n<p>\nVice President\n<\/p>\n<p>\nStallergenes Greer\n<\/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.\n<\/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.\n<\/p>\n<p>\nFor more information about this training visit <a target=\"_blank\" href=\"https:\/\/www.researchandmarkets.com\/reports\/5714341\/2-day-seminar-quality-and-gmp-compliance-for?utm_source=BW&amp;utm_medium=PressRelease&amp;utm_code=4cq3b8&amp;utm_campaign=1809638+-+2+Day+Seminar+Quality+and+GMP+Compliance+for+Virtual+Companies+(Pharmaceutical+and+Biologics+Industries)+(March+2-3%2C+2023)&amp;utm_exec=como322prd\" rel=\"nofollow noopener\" shape=\"rect\">https:\/\/www.researchandmarkets.com\/r\/vfx5yr<\/a>\n<\/p>\n<p>\n<strong>About ResearchAndMarkets.com<\/strong>\n<\/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.\n<\/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=\"&#x6d;&#97;&#105;l&#x74;&#x6f;&#58;p&#x72;&#x65;&#115;s&#x40;&#x72;&#101;s&#x65;&#x61;&#114;c&#x68;&#x61;&#110;d&#x6d;&#x61;&#114;&#107;e&#x74;&#x73;&#46;c&#x6f;&#x6d;\" rel=\"nofollow noopener\" shape=\"rect\">pre&#115;&#115;&#64;&#x72;&#x65;&#x73;&#x65;&#x61;&#x72;cha&#110;&#100;&#109;&#97;&#x72;&#x6b;&#x65;&#x74;&#x73;&#x2e;com<\/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\n<\/p>\n<\/div>\n","protected":false},"excerpt":{"rendered":"<p>DUBLIN&#8211;(BUSINESS WIRE)&#8211;The &#8220;2 Day Seminar Quality and GMP Compliance for Virtual Companies (Pharmaceutical and Biologics Industries)&#8221; training has been added to ResearchAndMarkets.com&#8217;s offering. Today, many companies operate on an outsourcing model. This is very common for companies who are evolving from being mainly development-focused to a point where they are entering latter stages of Phase &#8230; <span class=\"more\"><a class=\"more-link\" href=\"https:\/\/pharma-trend.com\/en\/2-day-seminar-quality-and-gmp-compliance-for-virtual-companies-pharmaceutical-and-biologics-industries-march-2-3-2023-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-53050","6":"format-standard","7":"category-industry"},"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.3 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>2 Day Seminar Quality and GMP Compliance for Virtual Companies (Pharmaceutical and Biologics Industries) (March 2-3, 2023) - 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\/2-day-seminar-quality-and-gmp-compliance-for-virtual-companies-pharmaceutical-and-biologics-industries-march-2-3-2023-researchandmarkets-com\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"2 Day Seminar Quality and GMP Compliance for Virtual Companies (Pharmaceutical and Biologics Industries) (March 2-3, 2023) - ResearchAndMarkets.com - Pharma Trend\" \/>\n<meta property=\"og:description\" content=\"DUBLIN&#8211;(BUSINESS WIRE)&#8211;The &#8220;2 Day Seminar Quality and GMP Compliance for Virtual Companies (Pharmaceutical and Biologics Industries)&#8221; training has been added to ResearchAndMarkets.com&#8217;s offering. Today, many companies operate on an outsourcing model. This is very common for companies who are evolving from being mainly development-focused to a point where they are entering latter stages of Phase ... [Read more...]\" \/>\n<meta property=\"og:url\" content=\"https:\/\/pharma-trend.com\/en\/2-day-seminar-quality-and-gmp-compliance-for-virtual-companies-pharmaceutical-and-biologics-industries-march-2-3-2023-researchandmarkets-com\/\" \/>\n<meta property=\"og:site_name\" content=\"Pharma Trend\" \/>\n<meta property=\"article:published_time\" content=\"2023-01-18T17:02:46+00:00\" \/>\n<meta property=\"og:image\" content=\"https:\/\/mms.businesswire.com\/media\/20230118005782\/en\/1689494\/21\/logo.jpg\" \/>\n<meta name=\"author\" content=\"Business Wire\" \/>\n<meta name=\"twitter:card\" content=\"summary_large_image\" \/>\n<meta name=\"twitter:label1\" content=\"Written by\" \/>\n\t<meta name=\"twitter:data1\" content=\"Business Wire\" \/>\n\t<meta name=\"twitter:label2\" content=\"Est. reading time\" \/>\n\t<meta name=\"twitter:data2\" content=\"5 minutes\" \/>\n<script type=\"application\/ld+json\" class=\"yoast-schema-graph\">{\"@context\":\"https:\\\/\\\/schema.org\",\"@graph\":[{\"@type\":\"Article\",\"@id\":\"https:\\\/\\\/pharma-trend.com\\\/en\\\/2-day-seminar-quality-and-gmp-compliance-for-virtual-companies-pharmaceutical-and-biologics-industries-march-2-3-2023-researchandmarkets-com\\\/#article\",\"isPartOf\":{\"@id\":\"https:\\\/\\\/pharma-trend.com\\\/en\\\/2-day-seminar-quality-and-gmp-compliance-for-virtual-companies-pharmaceutical-and-biologics-industries-march-2-3-2023-researchandmarkets-com\\\/\"},\"author\":{\"name\":\"Business Wire\",\"@id\":\"https:\\\/\\\/pharma-trend.com\\\/en\\\/#\\\/schema\\\/person\\\/02d41342c7a74fa7f0032bb35ef0bb24\"},\"headline\":\"2 Day Seminar Quality and GMP Compliance for Virtual Companies (Pharmaceutical and Biologics Industries) (March 2-3, 2023) &#8211; ResearchAndMarkets.com\",\"datePublished\":\"2023-01-18T17:02:46+00:00\",\"mainEntityOfPage\":{\"@id\":\"https:\\\/\\\/pharma-trend.com\\\/en\\\/2-day-seminar-quality-and-gmp-compliance-for-virtual-companies-pharmaceutical-and-biologics-industries-march-2-3-2023-researchandmarkets-com\\\/\"},\"wordCount\":1107,\"publisher\":{\"@id\":\"https:\\\/\\\/pharma-trend.com\\\/en\\\/#organization\"},\"image\":{\"@id\":\"https:\\\/\\\/pharma-trend.com\\\/en\\\/2-day-seminar-quality-and-gmp-compliance-for-virtual-companies-pharmaceutical-and-biologics-industries-march-2-3-2023-researchandmarkets-com\\\/#primaryimage\"},\"thumbnailUrl\":\"https:\\\/\\\/mms.businesswire.com\\\/media\\\/20230118005782\\\/en\\\/1689494\\\/21\\\/logo.jpg\",\"articleSection\":[\"Industry\"],\"inLanguage\":\"en-US\"},{\"@type\":\"WebPage\",\"@id\":\"https:\\\/\\\/pharma-trend.com\\\/en\\\/2-day-seminar-quality-and-gmp-compliance-for-virtual-companies-pharmaceutical-and-biologics-industries-march-2-3-2023-researchandmarkets-com\\\/\",\"url\":\"https:\\\/\\\/pharma-trend.com\\\/en\\\/2-day-seminar-quality-and-gmp-compliance-for-virtual-companies-pharmaceutical-and-biologics-industries-march-2-3-2023-researchandmarkets-com\\\/\",\"name\":\"2 Day Seminar Quality and GMP Compliance for Virtual Companies (Pharmaceutical and Biologics Industries) (March 2-3, 2023) - ResearchAndMarkets.com - Pharma Trend\",\"isPartOf\":{\"@id\":\"https:\\\/\\\/pharma-trend.com\\\/en\\\/#website\"},\"primaryImageOfPage\":{\"@id\":\"https:\\\/\\\/pharma-trend.com\\\/en\\\/2-day-seminar-quality-and-gmp-compliance-for-virtual-companies-pharmaceutical-and-biologics-industries-march-2-3-2023-researchandmarkets-com\\\/#primaryimage\"},\"image\":{\"@id\":\"https:\\\/\\\/pharma-trend.com\\\/en\\\/2-day-seminar-quality-and-gmp-compliance-for-virtual-companies-pharmaceutical-and-biologics-industries-march-2-3-2023-researchandmarkets-com\\\/#primaryimage\"},\"thumbnailUrl\":\"https:\\\/\\\/mms.businesswire.com\\\/media\\\/20230118005782\\\/en\\\/1689494\\\/21\\\/logo.jpg\",\"datePublished\":\"2023-01-18T17:02:46+00:00\",\"breadcrumb\":{\"@id\":\"https:\\\/\\\/pharma-trend.com\\\/en\\\/2-day-seminar-quality-and-gmp-compliance-for-virtual-companies-pharmaceutical-and-biologics-industries-march-2-3-2023-researchandmarkets-com\\\/#breadcrumb\"},\"inLanguage\":\"en-US\",\"potentialAction\":[{\"@type\":\"ReadAction\",\"target\":[\"https:\\\/\\\/pharma-trend.com\\\/en\\\/2-day-seminar-quality-and-gmp-compliance-for-virtual-companies-pharmaceutical-and-biologics-industries-march-2-3-2023-researchandmarkets-com\\\/\"]}]},{\"@type\":\"ImageObject\",\"inLanguage\":\"en-US\",\"@id\":\"https:\\\/\\\/pharma-trend.com\\\/en\\\/2-day-seminar-quality-and-gmp-compliance-for-virtual-companies-pharmaceutical-and-biologics-industries-march-2-3-2023-researchandmarkets-com\\\/#primaryimage\",\"url\":\"https:\\\/\\\/mms.businesswire.com\\\/media\\\/20230118005782\\\/en\\\/1689494\\\/21\\\/logo.jpg\",\"contentUrl\":\"https:\\\/\\\/mms.businesswire.com\\\/media\\\/20230118005782\\\/en\\\/1689494\\\/21\\\/logo.jpg\"},{\"@type\":\"BreadcrumbList\",\"@id\":\"https:\\\/\\\/pharma-trend.com\\\/en\\\/2-day-seminar-quality-and-gmp-compliance-for-virtual-companies-pharmaceutical-and-biologics-industries-march-2-3-2023-researchandmarkets-com\\\/#breadcrumb\",\"itemListElement\":[{\"@type\":\"ListItem\",\"position\":1,\"name\":\"Startseite\",\"item\":\"https:\\\/\\\/pharma-trend.com\\\/en\\\/\"},{\"@type\":\"ListItem\",\"position\":2,\"name\":\"2 Day Seminar Quality and GMP Compliance for Virtual Companies (Pharmaceutical and Biologics Industries) (March 2-3, 2023) &#8211; ResearchAndMarkets.com\"}]},{\"@type\":\"WebSite\",\"@id\":\"https:\\\/\\\/pharma-trend.com\\\/en\\\/#website\",\"url\":\"https:\\\/\\\/pharma-trend.com\\\/en\\\/\",\"name\":\"Pharma Trend\",\"description\":\"\",\"publisher\":{\"@id\":\"https:\\\/\\\/pharma-trend.com\\\/en\\\/#organization\"},\"potentialAction\":[{\"@type\":\"SearchAction\",\"target\":{\"@type\":\"EntryPoint\",\"urlTemplate\":\"https:\\\/\\\/pharma-trend.com\\\/en\\\/?s={search_term_string}\"},\"query-input\":{\"@type\":\"PropertyValueSpecification\",\"valueRequired\":true,\"valueName\":\"search_term_string\"}}],\"inLanguage\":\"en-US\"},{\"@type\":\"Organization\",\"@id\":\"https:\\\/\\\/pharma-trend.com\\\/en\\\/#organization\",\"name\":\"Pharma Trend\",\"url\":\"https:\\\/\\\/pharma-trend.com\\\/en\\\/\",\"logo\":{\"@type\":\"ImageObject\",\"inLanguage\":\"en-US\",\"@id\":\"https:\\\/\\\/pharma-trend.com\\\/en\\\/#\\\/schema\\\/logo\\\/image\\\/\",\"url\":\"\",\"contentUrl\":\"\",\"caption\":\"Pharma Trend\"},\"image\":{\"@id\":\"https:\\\/\\\/pharma-trend.com\\\/en\\\/#\\\/schema\\\/logo\\\/image\\\/\"}},{\"@type\":\"Person\",\"@id\":\"https:\\\/\\\/pharma-trend.com\\\/en\\\/#\\\/schema\\\/person\\\/02d41342c7a74fa7f0032bb35ef0bb24\",\"name\":\"Business Wire\"}]}<\/script>\n<!-- \/ Yoast SEO plugin. -->","yoast_head_json":{"title":"2 Day Seminar Quality and GMP Compliance for Virtual Companies (Pharmaceutical and Biologics Industries) (March 2-3, 2023) - ResearchAndMarkets.com - Pharma Trend","robots":{"index":"index","follow":"follow","max-snippet":"max-snippet:-1","max-image-preview":"max-image-preview:large","max-video-preview":"max-video-preview:-1"},"canonical":"https:\/\/pharma-trend.com\/en\/2-day-seminar-quality-and-gmp-compliance-for-virtual-companies-pharmaceutical-and-biologics-industries-march-2-3-2023-researchandmarkets-com\/","og_locale":"en_US","og_type":"article","og_title":"2 Day Seminar Quality and GMP Compliance for Virtual Companies (Pharmaceutical and Biologics Industries) (March 2-3, 2023) - ResearchAndMarkets.com - Pharma Trend","og_description":"DUBLIN&#8211;(BUSINESS WIRE)&#8211;The &#8220;2 Day Seminar Quality and GMP Compliance for Virtual Companies (Pharmaceutical and Biologics Industries)&#8221; training has been added to ResearchAndMarkets.com&#8217;s offering. Today, many companies operate on an outsourcing model. This is very common for companies who are evolving from being mainly development-focused to a point where they are entering latter stages of Phase ... [Read more...]","og_url":"https:\/\/pharma-trend.com\/en\/2-day-seminar-quality-and-gmp-compliance-for-virtual-companies-pharmaceutical-and-biologics-industries-march-2-3-2023-researchandmarkets-com\/","og_site_name":"Pharma Trend","article_published_time":"2023-01-18T17:02:46+00:00","og_image":[{"url":"https:\/\/mms.businesswire.com\/media\/20230118005782\/en\/1689494\/21\/logo.jpg","type":"","width":"","height":""}],"author":"Business Wire","twitter_card":"summary_large_image","twitter_misc":{"Written by":"Business Wire","Est. reading time":"5 minutes"},"schema":{"@context":"https:\/\/schema.org","@graph":[{"@type":"Article","@id":"https:\/\/pharma-trend.com\/en\/2-day-seminar-quality-and-gmp-compliance-for-virtual-companies-pharmaceutical-and-biologics-industries-march-2-3-2023-researchandmarkets-com\/#article","isPartOf":{"@id":"https:\/\/pharma-trend.com\/en\/2-day-seminar-quality-and-gmp-compliance-for-virtual-companies-pharmaceutical-and-biologics-industries-march-2-3-2023-researchandmarkets-com\/"},"author":{"name":"Business Wire","@id":"https:\/\/pharma-trend.com\/en\/#\/schema\/person\/02d41342c7a74fa7f0032bb35ef0bb24"},"headline":"2 Day Seminar Quality and GMP Compliance for Virtual Companies (Pharmaceutical and Biologics Industries) (March 2-3, 2023) &#8211; ResearchAndMarkets.com","datePublished":"2023-01-18T17:02:46+00:00","mainEntityOfPage":{"@id":"https:\/\/pharma-trend.com\/en\/2-day-seminar-quality-and-gmp-compliance-for-virtual-companies-pharmaceutical-and-biologics-industries-march-2-3-2023-researchandmarkets-com\/"},"wordCount":1107,"publisher":{"@id":"https:\/\/pharma-trend.com\/en\/#organization"},"image":{"@id":"https:\/\/pharma-trend.com\/en\/2-day-seminar-quality-and-gmp-compliance-for-virtual-companies-pharmaceutical-and-biologics-industries-march-2-3-2023-researchandmarkets-com\/#primaryimage"},"thumbnailUrl":"https:\/\/mms.businesswire.com\/media\/20230118005782\/en\/1689494\/21\/logo.jpg","articleSection":["Industry"],"inLanguage":"en-US"},{"@type":"WebPage","@id":"https:\/\/pharma-trend.com\/en\/2-day-seminar-quality-and-gmp-compliance-for-virtual-companies-pharmaceutical-and-biologics-industries-march-2-3-2023-researchandmarkets-com\/","url":"https:\/\/pharma-trend.com\/en\/2-day-seminar-quality-and-gmp-compliance-for-virtual-companies-pharmaceutical-and-biologics-industries-march-2-3-2023-researchandmarkets-com\/","name":"2 Day Seminar Quality and GMP Compliance for Virtual Companies (Pharmaceutical and Biologics Industries) (March 2-3, 2023) - ResearchAndMarkets.com - Pharma Trend","isPartOf":{"@id":"https:\/\/pharma-trend.com\/en\/#website"},"primaryImageOfPage":{"@id":"https:\/\/pharma-trend.com\/en\/2-day-seminar-quality-and-gmp-compliance-for-virtual-companies-pharmaceutical-and-biologics-industries-march-2-3-2023-researchandmarkets-com\/#primaryimage"},"image":{"@id":"https:\/\/pharma-trend.com\/en\/2-day-seminar-quality-and-gmp-compliance-for-virtual-companies-pharmaceutical-and-biologics-industries-march-2-3-2023-researchandmarkets-com\/#primaryimage"},"thumbnailUrl":"https:\/\/mms.businesswire.com\/media\/20230118005782\/en\/1689494\/21\/logo.jpg","datePublished":"2023-01-18T17:02:46+00:00","breadcrumb":{"@id":"https:\/\/pharma-trend.com\/en\/2-day-seminar-quality-and-gmp-compliance-for-virtual-companies-pharmaceutical-and-biologics-industries-march-2-3-2023-researchandmarkets-com\/#breadcrumb"},"inLanguage":"en-US","potentialAction":[{"@type":"ReadAction","target":["https:\/\/pharma-trend.com\/en\/2-day-seminar-quality-and-gmp-compliance-for-virtual-companies-pharmaceutical-and-biologics-industries-march-2-3-2023-researchandmarkets-com\/"]}]},{"@type":"ImageObject","inLanguage":"en-US","@id":"https:\/\/pharma-trend.com\/en\/2-day-seminar-quality-and-gmp-compliance-for-virtual-companies-pharmaceutical-and-biologics-industries-march-2-3-2023-researchandmarkets-com\/#primaryimage","url":"https:\/\/mms.businesswire.com\/media\/20230118005782\/en\/1689494\/21\/logo.jpg","contentUrl":"https:\/\/mms.businesswire.com\/media\/20230118005782\/en\/1689494\/21\/logo.jpg"},{"@type":"BreadcrumbList","@id":"https:\/\/pharma-trend.com\/en\/2-day-seminar-quality-and-gmp-compliance-for-virtual-companies-pharmaceutical-and-biologics-industries-march-2-3-2023-researchandmarkets-com\/#breadcrumb","itemListElement":[{"@type":"ListItem","position":1,"name":"Startseite","item":"https:\/\/pharma-trend.com\/en\/"},{"@type":"ListItem","position":2,"name":"2 Day Seminar Quality and GMP Compliance for Virtual Companies (Pharmaceutical and Biologics Industries) (March 2-3, 2023) &#8211; ResearchAndMarkets.com"}]},{"@type":"WebSite","@id":"https:\/\/pharma-trend.com\/en\/#website","url":"https:\/\/pharma-trend.com\/en\/","name":"Pharma Trend","description":"","publisher":{"@id":"https:\/\/pharma-trend.com\/en\/#organization"},"potentialAction":[{"@type":"SearchAction","target":{"@type":"EntryPoint","urlTemplate":"https:\/\/pharma-trend.com\/en\/?s={search_term_string}"},"query-input":{"@type":"PropertyValueSpecification","valueRequired":true,"valueName":"search_term_string"}}],"inLanguage":"en-US"},{"@type":"Organization","@id":"https:\/\/pharma-trend.com\/en\/#organization","name":"Pharma Trend","url":"https:\/\/pharma-trend.com\/en\/","logo":{"@type":"ImageObject","inLanguage":"en-US","@id":"https:\/\/pharma-trend.com\/en\/#\/schema\/logo\/image\/","url":"","contentUrl":"","caption":"Pharma Trend"},"image":{"@id":"https:\/\/pharma-trend.com\/en\/#\/schema\/logo\/image\/"}},{"@type":"Person","@id":"https:\/\/pharma-trend.com\/en\/#\/schema\/person\/02d41342c7a74fa7f0032bb35ef0bb24","name":"Business Wire"}]}},"_links":{"self":[{"href":"https:\/\/pharma-trend.com\/en\/wp-json\/wp\/v2\/posts\/53050","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/pharma-trend.com\/en\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/pharma-trend.com\/en\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/pharma-trend.com\/en\/wp-json\/wp\/v2\/users\/4"}],"replies":[{"embeddable":true,"href":"https:\/\/pharma-trend.com\/en\/wp-json\/wp\/v2\/comments?post=53050"}],"version-history":[{"count":0,"href":"https:\/\/pharma-trend.com\/en\/wp-json\/wp\/v2\/posts\/53050\/revisions"}],"wp:attachment":[{"href":"https:\/\/pharma-trend.com\/en\/wp-json\/wp\/v2\/media?parent=53050"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/pharma-trend.com\/en\/wp-json\/wp\/v2\/categories?post=53050"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/pharma-trend.com\/en\/wp-json\/wp\/v2\/tags?post=53050"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}