PRESS RELEASE
2 May 2025

Critical Medical Device Series: Part III Conducting Effective Due Diligence In MedTech Transactions

AP
Arnold & Porter

Contributor

Arnold & Porter is a firm of more than 1,000 lawyers, providing sophisticated litigation and transactional capabilities, renowned regulatory experience and market-leading multidisciplinary practices in the life sciences and financial services industries. Our global reach, experience and deep knowledge allow us to work across geographic, cultural, technological and ideological borders.
The MedTech industry is evolving and increasingly becoming subject to regulation and governmental scrutiny, resulting in unique legal and business challenges that present both substantial risk and reward.
United States

The MedTech industry is evolving and increasingly becoming subject to regulation and governmental scrutiny, resulting in unique legal and business challenges that present both substantial risk and reward.

Arnold & Porter partners Hemmie Chang and Phil Desjardins and senior associate Phil DeFedele will discuss how to mitigate and address major FDA regulatory, compliance, and business risks in MedTech transactions through effective due diligence and contractual and operational strategies. Whether you are focused on MedTech M&A or licensing deals, this program will provide you with insights on how to navigate these complex regulatory and business issues.

Webinar Series Alert

Part IV: IP Strategies for MedTech
Thursday, May 22
11 a.m.-noon ET

Contributor

Arnold & Porter is a firm of more than 1,000 lawyers, providing sophisticated litigation and transactional capabilities, renowned regulatory experience and market-leading multidisciplinary practices in the life sciences and financial services industries. Our global reach, experience and deep knowledge allow us to work across geographic, cultural, technological and ideological borders.

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