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This article analyzes how intellectual property portfolio management can simultaneously promote innovation and present potential...
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FDA’s September 2025 guidance requires detailed characterization of posttranslational modifications (PTMs), particularly glycosylation,...
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This article was originally published in the AIPLA Chemical Practice Chronicles Fall 2025 newsletter and is republished here with...
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USPTO Director Squires released updated guidance on AI-assisted inventions. The new guidance states that AI-assisted inventions are...
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That’s a wrap! We recently co-hosted TEDAI San Francisco, the most important global gathering for thought leadership in artificial...
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Artificial intelligence (AI) is transforming health care and biotechnology, propelling advancements in drug discovery, genomics, medical...
The USPTO announced a new pilot program designed to help it efficiently reduce the backlog of unexamined patent applications. The...
In what some are perceiving as the second blow of a one-two punch against patent trial proceedings conducted at the U.S. Patent and...
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The Long Life Family Study (LLFS) is a multi-decade, multicenter research program designed to uncover the genetic and biological factors...
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In the first proposed rulemaking issued under Director Squires, the USPTO proposes to modify the rules of practice relating to...
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On October 8, California Governor Newsom signed AB 566, which adds a section to the California Privacy Protection Agency (CCPA) to...
One of the goals of the new Director of the United States Patent and Trademark Office (USPTO) is to improve patent examination efficiency...
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For a decade, innovators at the intersection of artificial intelligence (AI) and precision medicine have faced a stubborn paradox: the...
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A Blueprint for FDA: Recommendations to Improve Innovation and Access [1] (FDA Blueprint) is a timely white paper authored by University...
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In Google v. Sonos, the Federal Circuit soundly disposed of arguments that the patent-in-suit was unenforceable due to laches based on an...
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Drug development can be slow, costly, and risky, often taking more than a decade and billions of dollars to bring a single therapy to the...