{"id":329,"date":"2022-08-08T11:52:44","date_gmt":"2022-08-08T15:52:44","guid":{"rendered":"https:\/\/blogs.duanemorris.com\/lifescienceslaw\/?p=329"},"modified":"2022-08-08T11:52:44","modified_gmt":"2022-08-08T15:52:44","slug":"coordinating-ip-and-regulatory-filings-can-minimize-the-risk-of-inequitable-conduct-before-the-pto","status":"publish","type":"post","link":"https:\/\/blogs.duanemorris.com\/lifescienceslaw\/2022\/08\/08\/coordinating-ip-and-regulatory-filings-can-minimize-the-risk-of-inequitable-conduct-before-the-pto\/","title":{"rendered":"Coordinating IP and Regulatory Filings Can Minimize the Risk of Inequitable Conduct Before the PTO"},"content":{"rendered":"<p>On July 29, 2022, the U.S. Patent and Trademark Office (PTO) published a Notice on the Duties of Disclosure and Reasonable Inquiry During Examination, Reexamination, and Reissue, and for Proceedings Before the Patent Trial and Appeal Board. The notice was part of the PTO\u2019s response to President Joe Biden\u2019s July 2021 Executive Order on Promoting Competition in the American Economy. It also answered Congress\u2019 call for PTO action following the Federal Circuit\u2019s September 2021 ruling that a drug formulation patent was unenforceable based on a drug manufacturer\u2019s inconsistent disclosures to both the PTO and the FDA. In view of the notice, companies should review the interface between their IP and regulatory functions to confirm that their interoperation (or lack thereof) does not run afoul of a patent applicant\u2019s duties of disclosure and reasonable inquiry to the PTO.<\/p>\n<p>To read the full text of this Duane Morris <em>Alert<\/em>, please <a href=\"https:\/\/www.duanemorris.com\/alerts\/coordinating_ip_regulatory_filings_can_minimize_risk_inequitable_conduct_before_pto_0822.html\" target=\"_blank\" rel=\"noopener\">visit the firm website<\/a>.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>On July 29, 2022, the U.S. Patent and Trademark Office (PTO) published a Notice on the Duties of Disclosure and Reasonable Inquiry During Examination, Reexamination, and Reissue, and for Proceedings Before the Patent Trial and Appeal Board. The notice was part of the PTO\u2019s response to President Joe Biden\u2019s July 2021 Executive Order on Promoting &hellip; <\/p>\n<p class=\"link-more\"><a href=\"https:\/\/blogs.duanemorris.com\/lifescienceslaw\/2022\/08\/08\/coordinating-ip-and-regulatory-filings-can-minimize-the-risk-of-inequitable-conduct-before-the-pto\/\" class=\"more-link\">Continue reading<span class=\"screen-reader-text\"> &#8220;Coordinating IP and Regulatory Filings Can Minimize the Risk of Inequitable Conduct Before the PTO&#8221;<\/span><\/a><\/p>\n","protected":false},"author":6,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[2],"tags":[594,620,619,78,329,545,274,544,547,105],"ppma_author":[521],"class_list":["post-329","post","type-post","status-publish","format-standard","hentry","category-general","tag-disclosures","tag-drug-formulation-patent","tag-executive-order","tag-federal-circuit","tag-generic-drugs","tag-patent-trial-and-appeal-board","tag-patents","tag-ptab","tag-u-s-patent-and-trademark-office","tag-uspto"],"authors":[{"term_id":521,"user_id":6,"is_guest":0,"slug":"duanemorris3","display_name":"Duane Morris","avatar_url":"https:\/\/secure.gravatar.com\/avatar\/843ff6e7a8fe5fc92109b47a45f34b6cf0ea499e6e788db23456c838b0ae6747?s=96&d=blank&r=g","author_category":"1","last_name":"Sullivan","first_name":"Margaret","job_title":"","user_url":"http:\/\/www.duanemorris.com","description":"<a href=\"http:\/\/www.duanemorris.com\">Visit the Duane Morris website.<\/a>"}],"_links":{"self":[{"href":"https:\/\/blogs.duanemorris.com\/lifescienceslaw\/wp-json\/wp\/v2\/posts\/329","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/blogs.duanemorris.com\/lifescienceslaw\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/blogs.duanemorris.com\/lifescienceslaw\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/blogs.duanemorris.com\/lifescienceslaw\/wp-json\/wp\/v2\/users\/6"}],"replies":[{"embeddable":true,"href":"https:\/\/blogs.duanemorris.com\/lifescienceslaw\/wp-json\/wp\/v2\/comments?post=329"}],"version-history":[{"count":0,"href":"https:\/\/blogs.duanemorris.com\/lifescienceslaw\/wp-json\/wp\/v2\/posts\/329\/revisions"}],"wp:attachment":[{"href":"https:\/\/blogs.duanemorris.com\/lifescienceslaw\/wp-json\/wp\/v2\/media?parent=329"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/blogs.duanemorris.com\/lifescienceslaw\/wp-json\/wp\/v2\/categories?post=329"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/blogs.duanemorris.com\/lifescienceslaw\/wp-json\/wp\/v2\/tags?post=329"},{"taxonomy":"author","embeddable":true,"href":"https:\/\/blogs.duanemorris.com\/lifescienceslaw\/wp-json\/wp\/v2\/ppma_author?post=329"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}