{"id":45274,"date":"2022-06-20T18:02:07","date_gmt":"2022-06-20T16:02:07","guid":{"rendered":"https:\/\/pharma-trend.com\/en\/eu-and-us-drug-product-batch-records-review-webinar-2022-researchandmarkets-com\/"},"modified":"2022-06-20T18:02:07","modified_gmt":"2022-06-20T16:02:07","slug":"eu-and-us-drug-product-batch-records-review-webinar-2022-researchandmarkets-com","status":"publish","type":"post","link":"https:\/\/pharma-trend.com\/en\/eu-and-us-drug-product-batch-records-review-webinar-2022-researchandmarkets-com\/","title":{"rendered":"EU and US Drug Product Batch Records Review Webinar 2022 &#8211; ResearchAndMarkets.com"},"content":{"rendered":"<div>\n<p>DUBLIN&#8211;(BUSINESS WIRE)&#8211;The <a target=\"_blank\" href=\"https:\/\/www.researchandmarkets.com\/reports\/5449087\/reviewing-drug-product-batch-records?utm_source=BW&amp;utm_medium=PressRelease&amp;utm_code=pkgtwn&amp;utm_campaign=1716172+-+EU+and+US+Drug+Product+Batch+Records+Review+Webinar+2022+&amp;utm_exec=chdo54prd\" rel=\"nofollow noopener\" shape=\"rect\">&#8220;Reviewing Drug Product Batch Records&#8221;<\/a> webinar has been added to <strong>ResearchAndMarkets.com&#8217;s<\/strong> offering.\n<\/p>\n<p><a href=\"https:\/\/mms.businesswire.com\/media\/20220620005445\/en\/1491330\/4\/logo.jpg\"><img decoding=\"async\" src=\"https:\/\/mms.businesswire.com\/media\/20220620005445\/en\/1491330\/21\/logo.jpg\"><\/a><\/p>\n<p>\nBatch record review is a GMP requirement. Furthermore, trending of manufacturing data facilitates continuous product improvement, which is the focus of a pending ICH guidance document (ICH Q12). Pharmaceutical manufacturers will be expected to demonstrate that their manufacturing processes continue to produce medicinal products of a consistently high quality.\n<\/p>\n<p>\nBatch records can also be used to identify sources of manufacturing variability, enabling improvements to be made to the production method. This webinar details current regulatory expectations and sets out a logical approach for batch record review. Methods for trending batch data will also be discussed. In addition to understanding regulatory expectations, you will learn how to use batch records as tools to facilitate continuous improvement.\n<\/p>\n<p>\n<strong>Who Should Attend:<\/strong>\n<\/p>\n<ul>\n<li>\nProduction staff\n<\/li>\n<li>\nProduction management\n<\/li>\n<li>\nQuality assurance professionals\n<\/li>\n<li>\nQualified persons (EU)\n<\/li>\n<li>\nRegulatory affairs professionals\n<\/li>\n<\/ul>\n<p>\n<strong>Key Topics Covered:<\/strong>\n<\/p>\n<ul>\n<li>\nRegulatory requirements for batch review (EU and US)\n<\/li>\n<li>\nImportant areas to check in batch records\n<\/li>\n<li>\nCommon errors\n<\/li>\n<li>\nExamples of deficiencies leading to regulatory enforcement action\n<\/li>\n<li>\nOverview of the draft ICH Q12 guidance\n<\/li>\n<li>\nICH Q12 and Quality by Design\n<\/li>\n<li>\nBenefits of continuous improvement\n<\/li>\n<li>\nApproaches to data trending\n<\/li>\n<\/ul>\n<p>\nFor more information about this webinar visit <a target=\"_blank\" href=\"https:\/\/www.researchandmarkets.com\/reports\/5449087\/reviewing-drug-product-batch-records?utm_source=BW&amp;utm_medium=PressRelease&amp;utm_code=pkgtwn&amp;utm_campaign=1716172+-+EU+and+US+Drug+Product+Batch+Records+Review+Webinar+2022+&amp;utm_exec=chdo54prd\" rel=\"nofollow noopener\" shape=\"rect\">https:\/\/www.researchandmarkets.com\/r\/uiq35l<\/a>\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;&#x61;&#x69;&#108;&#116;o:&#x70;&#x72;&#x65;&#x73;&#115;&#64;re&#x73;&#x65;&#x61;&#114;&#99;&#104;an&#x64;&#x6d;&#x61;&#114;&#107;et&#x73;&#x2e;&#x63;&#x6f;&#109;\" rel=\"nofollow noopener\" shape=\"rect\">&#112;r&#x65;s&#x73;&#64;&#x72;e&#x73;&#101;&#x61;&#114;&#x63;&#104;&#x61;&#110;d&#109;a&#x72;k&#x65;t&#x73;&#46;&#x63;&#111;&#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\n<\/p>\n<\/div>\n","protected":false},"excerpt":{"rendered":"<p>DUBLIN&#8211;(BUSINESS WIRE)&#8211;The &#8220;Reviewing Drug Product Batch Records&#8221; webinar has been added to ResearchAndMarkets.com&#8217;s offering. Batch record review is a GMP requirement. Furthermore, trending of manufacturing data facilitates continuous product improvement, which is the focus of a pending ICH guidance document (ICH Q12). Pharmaceutical manufacturers will be expected to demonstrate that their manufacturing processes continue to &#8230; <span class=\"more\"><a class=\"more-link\" href=\"https:\/\/pharma-trend.com\/en\/eu-and-us-drug-product-batch-records-review-webinar-2022-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-45274","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>EU and US Drug Product Batch Records Review Webinar 2022 - 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\/eu-and-us-drug-product-batch-records-review-webinar-2022-researchandmarkets-com\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"EU and US Drug Product Batch Records Review Webinar 2022 - ResearchAndMarkets.com - Pharma Trend\" \/>\n<meta property=\"og:description\" content=\"DUBLIN&#8211;(BUSINESS WIRE)&#8211;The &#8220;Reviewing Drug Product Batch Records&#8221; webinar has been added to ResearchAndMarkets.com&#8217;s offering. Batch record review is a GMP requirement. Furthermore, trending of manufacturing data facilitates continuous product improvement, which is the focus of a pending ICH guidance document (ICH Q12). Pharmaceutical manufacturers will be expected to demonstrate that their manufacturing processes continue to ... [Read more...]\" \/>\n<meta property=\"og:url\" content=\"https:\/\/pharma-trend.com\/en\/eu-and-us-drug-product-batch-records-review-webinar-2022-researchandmarkets-com\/\" \/>\n<meta property=\"og:site_name\" content=\"Pharma Trend\" \/>\n<meta property=\"article:published_time\" content=\"2022-06-20T16:02:07+00:00\" \/>\n<meta property=\"og:image\" content=\"https:\/\/mms.businesswire.com\/media\/20220620005445\/en\/1491330\/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=\"1 minute\" \/>\n<script type=\"application\/ld+json\" class=\"yoast-schema-graph\">{\"@context\":\"https:\\\/\\\/schema.org\",\"@graph\":[{\"@type\":\"Article\",\"@id\":\"https:\\\/\\\/pharma-trend.com\\\/en\\\/eu-and-us-drug-product-batch-records-review-webinar-2022-researchandmarkets-com\\\/#article\",\"isPartOf\":{\"@id\":\"https:\\\/\\\/pharma-trend.com\\\/en\\\/eu-and-us-drug-product-batch-records-review-webinar-2022-researchandmarkets-com\\\/\"},\"author\":{\"name\":\"Business Wire\",\"@id\":\"https:\\\/\\\/pharma-trend.com\\\/en\\\/#\\\/schema\\\/person\\\/02d41342c7a74fa7f0032bb35ef0bb24\"},\"headline\":\"EU and US Drug Product Batch Records Review Webinar 2022 &#8211; 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