{"id":925,"date":"2023-03-17T10:20:00","date_gmt":"2023-03-17T08:20:00","guid":{"rendered":"https:\/\/www.quadpharma.com\/qd\/?page_id=925"},"modified":"2023-03-17T10:21:36","modified_gmt":"2023-03-17T08:21:36","slug":"audit-inspection-of-third-party-sterile-manufacturers","status":"publish","type":"page","link":"https:\/\/www.quadpharma.com\/qd\/audit-inspection-of-third-party-sterile-manufacturers\/","title":{"rendered":"AUDIT\/Inspection of Third-Party Sterile Manufacturers"},"content":{"rendered":"\n<p class=\"wp-block-paragraph\"><strong>AUDIT\/Inspection of Third-Party Sterile Manufacturers<\/strong>:  \u00bd Day Workshop for Applicants based on PIC\/S GMP requirements<\/p>\n\n\n\n<p class=\"wp-block-paragraph\"><strong><u>Topics covered<\/u><\/strong><\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Where and why additional care must be taken for manufacture of sterile products<\/li>\n\n\n\n<li>Important elements of the sterile manufacturing facility<\/li>\n\n\n\n<li>Requirements for inspection of manufacturers that produce sterile dosage forms according to PIC\/S GMP, specifically Annex 1<\/li>\n\n\n\n<li>Guidelines and tips for inspection of manufacturers producing dosage forms such as Eye Drops, Injections and Infusions<\/li>\n<\/ul>\n\n\n\n<p class=\"wp-block-paragraph\"><strong><u>Learning Objectives<\/u><\/strong><\/p>\n\n\n\n<p class=\"wp-block-paragraph\">After the workshop, the learner will have an understanding of<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Where and why additional care must be taken for manufacture of sterile products<\/li>\n\n\n\n<li>Important elements of the sterile manufacturing facility<\/li>\n\n\n\n<li>Requirements for inspection of manufacturers that produce sterile dosage forms according to PIC\/S GMP, specifically Annex 1<\/li>\n\n\n\n<li>Tips on specific things to consider for inspecting manufacturers of sterile products<\/li>\n<\/ul>\n\n\n\n<p class=\"wp-block-paragraph\">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 Sterile Manufacturers: \u00bd 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 RA positions<\/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-925","page","type-page","status-publish","hentry"],"_links":{"self":[{"href":"https:\/\/www.quadpharma.com\/qd\/wp-json\/wp\/v2\/pages\/925","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=925"}],"version-history":[{"count":2,"href":"https:\/\/www.quadpharma.com\/qd\/wp-json\/wp\/v2\/pages\/925\/revisions"}],"predecessor-version":[{"id":927,"href":"https:\/\/www.quadpharma.com\/qd\/wp-json\/wp\/v2\/pages\/925\/revisions\/927"}],"wp:attachment":[{"href":"https:\/\/www.quadpharma.com\/qd\/wp-json\/wp\/v2\/media?parent=925"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}