On July 3, 2020, the Standing Committee of the National People’s Congress (“NPC”) of China published a second draft amendment (the “Draft”) on the Patent Law of the People’s Republic of China (“Patent Law”). Most notably among the Draft’s proposed 29 revisions to the Patent Law, the Draft includes high-level provisions that would establish a framework for early resolution of pharmaceutical patent disputes between patentees and interested parties of approved drug products and applicants for follow-on drug products,1 often referred to as a patent linkage system. Specifically, the Draft includes new provisions that could create a jurisdictional basis—both for civil and administrative proceedings—for early resolution of patent infringement disputes involving a marketed drug product, and might establish a nine-month stay of approval of the follow-on application while the patent dispute is being adjudicated. The Draft also introduces high-level provisions that would establish patent term adjustment (“PTA”) and, for “invention patents of new drugs,” patent term restoration (“PTR”) regimes.

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Photo of Ruixue Ran Ruixue Ran

Ruixue Ran is the managing partner of Covington’s Beijing office and a member of Patent Litigation Practice Group. She specializes in U.S. Section 337 investigations (“ITC practice”) and intellectual property litigation (“IP litigation”). Her practice has involved cases spanning a wide range of

Ruixue Ran is the managing partner of Covington’s Beijing office and a member of Patent Litigation Practice Group. She specializes in U.S. Section 337 investigations (“ITC practice”) and intellectual property litigation (“IP litigation”). Her practice has involved cases spanning a wide range of claims, including patent, trade secrets, trademark, and other types of unfair competition.

A pioneer ITC practitioner in China, Ruixue is among the few lawyers who have consistently handled Section 337 cases on behalf of Chinese companies over the years and has substantial experience in representing Chinese companies in high-stakes IP litigation before the ITC and U.S. courts. Her representative cases include the historic litigation victory for Baosteel and China’s steel industry in all three claims of the Section 337 Steel case  (Inv. No. 337-TA-1002). She further serves as coordinating counsel for Chinese companies’ complex IP litigations in multiple jurisdictions, including but not limited to the U.S., EU, and China.

In addition, she helps multinational clients navigate cross-border IP litigations involving China and coordinates legal proceedings outside of China with overall global IP strategy. With integrated litigation experience in China and U.S., she has succeeded in resolving international companies’ high profile disputes in China.

Ruixue’s successful representation of clients has drawn upon her rich work experience in both U.S. and Chinese law firms, U.S. and Chinese companies, and the Chinese government, as well as her in-depth understanding of the hi-tech and manufacturing sectors.

Asian Legal Business named her one of the “Top 15 Female Lawyers in China” in 2015 and one of the “Top 15 IP Lawyers in China” in 2016. China Law & Practice named her the IP Lawyer of the Year in 2018. IAM Patent 1000 named her a “leading patent individual” (2022).

Photo of John Balzano John Balzano

John Balzano represents companies and business associations on U.S. and China regulatory and policy matters related to food, drugs, medical devices, cosmetics, and other regulated products.

John has over a decade of experience with legal and regulatory issues related to China, particularly with…

John Balzano represents companies and business associations on U.S. and China regulatory and policy matters related to food, drugs, medical devices, cosmetics, and other regulated products.

John has over a decade of experience with legal and regulatory issues related to China, particularly with regard to products regulated by the State Administration for Market Regulation, the National Medical Products Administration (NMPA), and other agriculture, animal and healthcare (including digital health) products and services. He assists clients with developing strategies to obtain pre-market approvals for these products in China, including clinical development, understanding relevant pricing and reimbursement policies, and reviewing distribution and promotional plans.

He also advises on regulatory compliance, due diligence, and enforcement matters for China operations, including drafting and revising and integrating China and global standard operating procedures, assessing the functions of regulatory departments in China, responding to inspection results and enforcement inquiries, and implementing product recalls. John also has significant experience designing strategies to handle professional consumer litigation for food and cosmetic companies operating in China and working with local counsel.

He advises companies and industry associations on their advocacy strategies, including the notice and comment process before NMPA and other regulatory agencies.

John has particular experience in the U.S. advising on the requirements for the acquisition and transfer of biospecimens for research purposes.

Photo of Sheng Huang Sheng Huang

Sheng Huang is of counsel in the firm’s Beijing office. He focuses on China-related practices. He has extensive experience in intellectual property law, specializing in the resolution of Chinese companies’ cross-border intellectual property disputes.

He also assisted international and Chinese clients with their…

Sheng Huang is of counsel in the firm’s Beijing office. He focuses on China-related practices. He has extensive experience in intellectual property law, specializing in the resolution of Chinese companies’ cross-border intellectual property disputes.

He also assisted international and Chinese clients with their intellectual property issues in China.

Photo of Julia Post Julia Post

Julia Post advises companies and trade associations on a broad range of regulatory and policy matters related to drugs, biologics, and other regulated products in both the U.S. and China. Julia has significant experience in advising clients on clinical trial and product development…

Julia Post advises companies and trade associations on a broad range of regulatory and policy matters related to drugs, biologics, and other regulated products in both the U.S. and China. Julia has significant experience in advising clients on clinical trial and product development matters, including informed consent requirements, biospecimen procurement and research use, and other good clinical practice. She advises clients regularly on product life-cycle management issues, including patent linkage frameworks and marketing exclusivity in the U.S. and China.

Julia works with pharmaceutical, medical device, food, and cosmetics clients on complex regulatory compliance matters and helps them develop their advocacy strategies before U.S. and China regulators, at both national and local levels. She regularly assists companies and trade associations on policy issues, including the development and submission of comments on legislative and regulatory proposals. Julia works closely with local counsel throughout the Asia-Pacific region to assist clients with their marketing approval and compliance strategies.

Prior to joining the Food, Drug, and Device practice group, Julia was a member of the Litigation practice group where she focused on representing clients in Hatch-Waxman patent litigation.

Julia has an active pro bono practice at Covington, with a particular focus on reproductive justice matters and representation of third-party caregivers and children in custody cases.