Li-Hsien (Lily) Rin-Laures, M.D.
Partner
For clients in the biopharma industry, Li-Hsien (Lily) Rin-Laures, M.D. is a strategic partner in using intellectual property to achieve her clients’ business goals. With two decades of experience in building and assessing patent portfolios in the biopharma industry, as well as in negotiating licenses and strategic alliances, she anticipates issues and opportunities. She brings to her practice a unique insider’s perspective gained as former General Counsel of a publicly held biotechnology company, and insight acquired from managing patent portfolios for a number of FDA-approved drugs. A substantial part of her work involves the interface of patents with clinical product development, FDA regulations and regulatory exclusivity.
Recent Client Work
- Worked creatively and closely with attorneys and scientists at different companies to obtain patent protection covering several approved drugs.
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Successfully argued an appeal before the U.S. Patent Office’s Board of Patent Appeals and Interferences on claims covering a commercially successful FDA-approved drug.
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Persistently pursued patent applications relating to an FDA-approved drug through appeals, interference and an appeal to the Court of Appeals for the Federal Circuit.
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Partnered with a company’s management team to craft worldwide IP strategy, and led IP interactions with collaborators.
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Negotiated the IP aspects of a collaboration alliance agreement with a large pharmaceutical company, and drafted and helped negotiate many licenses and other agreements.
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Advised on due diligence, valuation of patent portfolios and freedom-to-operate issues.
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Provided IP opinions to support securities offerings.
Li-Hsien (Lily) Rin-Laures, M.D.
Partner
For clients in the biopharma industry, Li-Hsien (Lily) Rin-Laures, M.D. is a strategic partner in using intellectual property to achieve her clients’ business goals. With two decades of experience in building and assessing patent portfolios in the biopharma industry, as well as in negotiating licenses and strategic alliances, she anticipates issues and opportunities. She brings to her practice a unique insider’s perspective gained as former General Counsel of a publicly held biotechnology company, and insight acquired from managing patent portfolios for a number of FDA-approved drugs. A substantial part of her work involves the interface of patents with clinical product development, FDA regulations and regulatory exclusivity.
- T.312.474.6641
- F.312.474.0448


Recent Client Work
- Worked creatively and closely with attorneys and scientists at different companies to obtain patent protection covering several approved drugs.
-
Successfully argued an appeal before the U.S. Patent Office’s Board of Patent Appeals and Interferences on claims covering a commercially successful FDA-approved drug.
-
Persistently pursued patent applications relating to an FDA-approved drug through appeals, interference and an appeal to the Court of Appeals for the Federal Circuit.
-
Partnered with a company’s management team to craft worldwide IP strategy, and led IP interactions with collaborators.
-
Negotiated the IP aspects of a collaboration alliance agreement with a large pharmaceutical company, and drafted and helped negotiate many licenses and other agreements.
-
Advised on due diligence, valuation of patent portfolios and freedom-to-operate issues.
-
Provided IP opinions to support securities offerings.


