{"id":92,"date":"2019-10-27T09:47:52","date_gmt":"2019-10-27T13:47:52","guid":{"rendered":"http:\/\/www.cloudstaffingpro.com\/bloga\/?p=92"},"modified":"2023-06-06T12:30:05","modified_gmt":"2023-06-06T16:30:05","slug":"fda-guidance-documents","status":"publish","type":"post","link":"https:\/\/www.cloudstaffingpro.com\/bloga\/fda-guidance-documents\/","title":{"rendered":"FDA Guidance\u200b Documents"},"content":{"rendered":"\n<p><strong>The US FDA has produced the A-List of Guidance Documents that CDRH intends to publish in FY2020.&nbsp;<\/strong><\/p>\n\n\n\n<p><strong>A-List: Prioritized Guidance Documents for FY2020&nbsp;<\/strong><\/p>\n\n\n\n<p>Final Guidance Topics<\/p>\n\n\n\n<ul><li>Select Updates for Recommendations for Clinical Laboratory Improvement Amendments of 1988 (CLIA) Waiver Applications for Manufacturers of In Vitro Diagnostic Devices<\/li><li>Recommendations for Dual 510(k) and Clinical Laboratory Improvement Amendments Waiver by Application Studies<\/li><li>510(k) Third Party Review Program<\/li><li>Safer Technologies Program for Medical Devices<\/li><li>Process to Request a Review of FDA&#8217;s Decision Not to Issue Certain Export Certificates for Devices<\/li><li>Labeling Recommendations for Surgical Staplers<\/li><li>Nonbinding Feedback After Certain Food and Drug Administration Inspections of Device Establishments<\/li><li>The Accreditation Scheme for Conformity Assessment (ASCA) Pilot Program<\/li><li>Recognition and Withdrawal of Voluntary Consensus Standards<\/li><li>Clinical Decision Support Software<\/li><li>Multiple Function Device Products: Policy and Considerations<\/li><li>Device-Specific Criteria Guidance(s) for Safety and Performance Based Pathway Implementation<\/li><\/ul>\n","protected":false},"excerpt":{"rendered":"<p>The US FDA has produced the A-List of Guidance Documents that CDRH intends to publish in FY2020.&nbsp; A-List: Prioritized Guidance Documents for FY2020&nbsp; Final Guidance Topics Select Updates for Recommendations for Clinical Laboratory Improvement Amendments of 1988 (CLIA) Waiver Applications for Manufacturers of In Vitro Diagnostic Devices Recommendations for Dual 510(k) and Clinical Laboratory Improvement [&hellip;]<\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"_coblocks_attr":"","_coblocks_dimensions":"","_coblocks_responsive_height":"","_coblocks_accordion_ie_support":""},"categories":[111,1],"tags":[],"_links":{"self":[{"href":"https:\/\/www.cloudstaffingpro.com\/bloga\/wp-json\/wp\/v2\/posts\/92"}],"collection":[{"href":"https:\/\/www.cloudstaffingpro.com\/bloga\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.cloudstaffingpro.com\/bloga\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.cloudstaffingpro.com\/bloga\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/www.cloudstaffingpro.com\/bloga\/wp-json\/wp\/v2\/comments?post=92"}],"version-history":[{"count":1,"href":"https:\/\/www.cloudstaffingpro.com\/bloga\/wp-json\/wp\/v2\/posts\/92\/revisions"}],"predecessor-version":[{"id":93,"href":"https:\/\/www.cloudstaffingpro.com\/bloga\/wp-json\/wp\/v2\/posts\/92\/revisions\/93"}],"wp:attachment":[{"href":"https:\/\/www.cloudstaffingpro.com\/bloga\/wp-json\/wp\/v2\/media?parent=92"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.cloudstaffingpro.com\/bloga\/wp-json\/wp\/v2\/categories?post=92"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.cloudstaffingpro.com\/bloga\/wp-json\/wp\/v2\/tags?post=92"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}