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Financial Regulations in Football: Caught Offside?

This article discusses the application of the current financial regulations (including PSR) to PL clubs and recent trends in compliance with these regulations, and examines certain aspects of the current regulations that the regulators could look to improve upon to deal with issues that arise from creative accounting practices and misaligned incentives.

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Challenges to Quantifying Economic Harm from Data Breaches

Quantifying economic harm resulting from data breaches is challenging. It requires sound economic analysis to address a range of issues, including issues related to personal data exposure and the valuation of privacy, the use of dark-web data for benchmarking, and the difficulties in assessing mitigation costs for class-action lawsuits.

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Ranked #1 in Global Arbitration Review’s 2024 Expert Witness Firms’ Power Index, Secretariat’s experts have extensive knowledge of the key issues important to government agencies, arbitration panels, regulators, legal counsel, and business leaders.

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News  |  October 16, 2024

UK Economic Crime and Corporate Transparency Act (ECCTA) Article Series

In this series of articles for Governance & Compliance magazine, Secretariat Managing Director Hitesh Patel and Director Ben Boorer explore the extensive reach and practical implications of the ECCTA, providing insights into how businesses can effectively navigate the challenges imposed by the ECCTA.

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Article  |  October 15, 2024

Ex Parte Proceedings — You’ll Never Walk Alone (They Said)

In an article for CICES 2024/2025 Construction Law Review, Associate Director Daniel Shaw shares lessons learned from his recent ex parte experience in ICC arbitration and discusses the roles of both the expert and the tribunal in ex parte proceedings.

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Biopharmaceutical Reasonable Royalties on Trial

When our client, a biopharmaceutical company, had exclusively licensed a patent for a novel type of cancer immunotherapy, a competitor undertook substantial efforts to be first to market for its lead indication despite being aware of potential infringement claims against its therapy. Upon the competitor achieving FDA approval, our client filed patent infringement claims. After an eight-day trial, the jury returned a verdict in favor of our client with a damages award that precisely matched the trial testimony.

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