Category: Bilateral Dialogues

QBPC, RDPAC and Distinct Foreign Voices in China’s IP System

The closure of the Quality Brands Protection Committee (QBPC) and the apparent absorption of the Research and Development Pharmaceutical Association Committee of China (RDPAC) into new institutional structures marks the end of an important chapter in the development of China’s modern intellectual property system. Founded during China’s WTO-accession era, both organizations played influential roles in fostering dialogue, advancing legal and regulatory reforms, and helping foreign and Chinese stakeholders identify areas of common interest. Drawing on examples ranging from anti-counterfeiting enforcement to pharmaceutical intellectual property reform, this article argues that their effectiveness often stemmed not from exerting pressure, but from aligning foreign experience with China’s evolving development priorities. Their disappearance reflects China’s transformation from a country primarily concerned with protecting foreign intellectual property into one with its own powerful innovation constituency. At the same time, it raises important questions about whether newer institutions can continue to represent concerns that uniquely affect foreign companies while preserving the technical exchanges, professional engagement, and practical cooperation that contributed to decades of intellectual property reform.

Post-Filing Data in Chinese Pharma Patents: Why It Took So Long — and What Finally Worked

Recently, the Supreme People’s Court of China (SPC) upheld a decision of the Beijing Intellectual Property Court reversing a China National Intellectual Property Administration (CNIPA) invalidation decision and confirming the validity of Novo Nordisk’s semaglutide compound patent. Although the final written decision has not yet been publicly released, official summaries indicate that the court accepted post-filing experimental data where “the technical effect can be derived from the original specification” (技术效果可由原说明书得出), reversing an administrative invalidation decision. Public reporting further indicates that the dispute turned on whether CNIPA would accept post-filing experimental data demonstrating semaglutide’s surprising pharmacokinetic effects in animal models, where the application as filed contained no experimental data.