{"id":923,"date":"2023-03-17T10:19:22","date_gmt":"2023-03-17T08:19:22","guid":{"rendered":"https:\/\/www.quadpharma.com\/qd\/?page_id=923"},"modified":"2023-03-17T10:19:24","modified_gmt":"2023-03-17T08:19:24","slug":"audit-inspection-of-third-party-manufacturers-excluding-sterile-dosage-forms","status":"publish","type":"page","link":"https:\/\/www.quadpharma.com\/qd\/audit-inspection-of-third-party-manufacturers-excluding-sterile-dosage-forms\/","title":{"rendered":"AUDIT\/Inspection of Third-Party Manufacturers (excluding sterile dosage forms)"},"content":{"rendered":"\n<p><strong>AUDIT\/Inspection of Third-Party Manufacturers (excluding sterile dosage forms<\/strong>): 1-day Workshop for Applicants based on PIC\/S GMP requirements<\/p>\n\n\n\n<p><strong><u>Topics covered<\/u><\/strong><\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Requirements for Third-Party Manufacturer Inspections according to PIC\/S GMP<\/li>\n\n\n\n<li>SAHPRA expectations regarding inspections of Third-Party Manufacturers by applicants<\/li>\n\n\n\n<li>What should be inspected according to the PIC\/S GMP guideline<\/li>\n\n\n\n<li>Guidelines and tips for inspection of manufacturers producing specific dosage forms such as Tablets, Capsules, Creams, Ointments, Effervescent Powders, Suspensions and Liquids<\/li>\n<\/ul>\n\n\n\n<p><strong><u>Learning Objectives<\/u><\/strong><\/p>\n\n\n\n<p>After the workshop, the learner will have an understanding of<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Why and when 3<sup>rd<\/sup> Party Manufacturers must be inspected<\/li>\n\n\n\n<li>What is the expectation of SAHPRA in terms of 3<sup>rd<\/sup> Party Manufacturer Inspection by applicants<\/li>\n\n\n\n<li>What guidelines can be used to aid 3rd Party Manufacturer inspections<\/li>\n\n\n\n<li>The inspection process<\/li>\n\n\n\n<li>How to use the PIC\/S GMP guideline and Annexes to conduct an inspection<\/li>\n\n\n\n<li>Important inspection points for specific dosage forms: Tablets, Capsules, Creams, Ointments, Effervescent Powders, Suspensions and Liquids<\/li>\n<\/ul>\n\n\n\n<p>The course is suitable for personnel in QA or RA positions with minimal manufacturing or inspection experience or exposure.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>AUDIT\/Inspection of Third-Party Manufacturers (excluding sterile dosage forms): 1-day Workshop for Applicants based on PIC\/S GMP requirements Topics covered Learning Objectives After the workshop, the learner will have an understanding of The course is suitable for personnel in QA or<\/p>\n","protected":false},"author":1,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"footnotes":""},"class_list":["post-923","page","type-page","status-publish","hentry"],"_links":{"self":[{"href":"https:\/\/www.quadpharma.com\/qd\/wp-json\/wp\/v2\/pages\/923","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.quadpharma.com\/qd\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/www.quadpharma.com\/qd\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/www.quadpharma.com\/qd\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/www.quadpharma.com\/qd\/wp-json\/wp\/v2\/comments?post=923"}],"version-history":[{"count":1,"href":"https:\/\/www.quadpharma.com\/qd\/wp-json\/wp\/v2\/pages\/923\/revisions"}],"predecessor-version":[{"id":924,"href":"https:\/\/www.quadpharma.com\/qd\/wp-json\/wp\/v2\/pages\/923\/revisions\/924"}],"wp:attachment":[{"href":"https:\/\/www.quadpharma.com\/qd\/wp-json\/wp\/v2\/media?parent=923"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}