{"id":2538,"date":"2021-05-19T08:40:18","date_gmt":"2021-05-19T08:40:18","guid":{"rendered":"https:\/\/www.pharmig.org.uk\/en\/?post_type=product&#038;p=2538"},"modified":"2025-12-05T19:26:11","modified_gmt":"2025-12-05T19:26:11","slug":"best-practices-for-out-of-specification-oos-investigations","status":"publish","type":"product","link":"https:\/\/www.pharmig.org.uk\/en\/product\/best-practices-for-out-of-specification-oos-investigations\/","title":{"rendered":"Best practices for out-of-specification (OOS) investigations"},"content":{"rendered":"<p>Fees: \u00a370 PHARMIG MEMBERS <a href=\"https:\/\/www.pharmig.org.uk\/en\/join-now\/\">Join Now<\/a>, \u00a0\u00a3100 (Non Member)<\/p>\n<p>The Zoom session will last for 60 minutes and include a Q&amp;A section<\/p>\n<h2>Webinar Outline<\/h2>\n<p class=\"red-span\"><strong>Best practices for out-of-specification (OOS) investigations<\/strong> Led by Dr Tim Sandle<\/p>\n<p><strong>Tuesday 29th June @3pm BST<\/strong><\/p>\n<p>This presentation looks at the best practices for laboratory out of specification (OOS) investigations. The OOS approach discussed will relate to both microbiological and chemical test samples.<\/p>\n<ul>\n<li>What makes for a good and a bad OOS investigation?<\/li>\n<li>What needs to be done for the different OOS phases?<\/li>\n<li>How can laboratory errors be assessed?<\/li>\n<li>How and OOS\u2019s be trended?<\/li>\n<li>What is needed for robust hypothesis testing?<\/li>\n<li>What needs to be considered for a production or process investigation?<\/li>\n<li>How should the OOS be documented?<\/li>\n<\/ul>\n<p><a href=\"https:\/\/www.pharmig.org.uk\/en\/wp-content\/uploads\/2021\/02\/Pharmigs-current-series-of-webinars-for-2021-MASTER-2.pdf\" target=\"_blank\" rel=\"noopener noreferrer\">Click on this link to download the booking form<\/a> and email back to <a href=\"mailto:info@pharmig.org.uk\" target=\"_blank\" rel=\"noopener noreferrer\">info@pharmig.org.uk<\/a> or book and pay through the website.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Fees: \u00a370 PHARMIG MEMBERS Join Now, \u00a0\u00a3100 (Non Member) The Zoom session will last for 60 minutes and include a Q&amp;A section Webinar Outline Best practices for out-of-specification (OOS) investigations Led by Dr Tim Sandle Tuesday 29th June @3pm BST This presentation looks at the best practices for laboratory out of specification (OOS) investigations. The [&hellip;]<\/p>\n","protected":false},"featured_media":460,"comment_status":"closed","ping_status":"closed","template":"","meta":{"pmpro_default_level":""},"product_brand":[],"product_cat":[41],"product_tag":[],"class_list":["post-2538","product","type-product","status-publish","has-post-thumbnail","product_cat-webinars-archive","pa_date-29th-june-3pm-bst","pmpro-has-access","first","instock","virtual","purchasable","product-type-simple"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v28.1 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Out-of-Spec Investigations: Best Practices (Pharma)<\/title>\n<meta name=\"description\" content=\"Best practices for out of specification investigations offers clear steps to help teams improve root-cause analysis, accuracy and compliance.\" \/>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" 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