Securing the Value of Life Sciences Acquisitions: Managing Foreign Investment Clearance and IP Risk | Kisaco Research

High-value life science acquisitions seldom occur without scrutiny. As governments increasingly treat advanced biotechnology, pharmaceutical manufacturing capabilities and proprietary research platforms as strategically sensitive assets, cross-border transactions in the sector are more likely than ever to trigger foreign investment screening and national security review. At the same time, the core patent portfolios, platform technologies and regulatory data packages driving these deals often attract immediate attention from competitors seeking to challenge the strength and scope of acquired IP before commercial launch.

This session will examine how legal teams safeguard the value of life science acquisitions by navigating foreign investment clearance processes while proactively managing the IP risks associated with newly acquired technologies. Bringing together corporate and IP perspectives, the discussion will explore how your company can structure transactions and prepare for potential IP challenges that may arise once high-profile acquisitions become public.

- When do life science acquisitions trigger foreign investment screening, and how can companies manage the resulting deal approval risk?
- How do regulators assess transactions involving strategically important life science technologies and IP portfolios?
- How can legal teams identify vulnerabilities in acquired patent portfolios and assess FTO risks before completing a transaction?
- What early IP and legal measures need to be put in place to protect newly acquired products?
- How should legal teams coordinate post acquisition to safeguard exclusivity and maximise the long-term value of acquired assets?

Speaker(s): 

Author:

Sophie Pelé

Partner
Dechert

Sophie Pelé, a partner in Dechert's Paris office, advises in life sciences regulatory matters. She also covers foreign investment control in international transactions and strategic public law litigation.

Ranked among the leading partners in Pharma/Life Sciences: Regulatory by Chambers France 2026, recognized as a “Next Generation Partner” in France by The Legal 500 EMEA 2026 in Healthcare & Life Sciences, as well as among the best lawyers in Life Sciences by Who’s Who Legal 2025, Sophie Pelé has substantial experience in clinical trial, development, manufacturing and promotion agreements, licensing and distribution schemes, market access transparency, lifecycle management, and hospital-related public procurement.

Sophie Pelé

Partner
Dechert

Sophie Pelé, a partner in Dechert's Paris office, advises in life sciences regulatory matters. She also covers foreign investment control in international transactions and strategic public law litigation.

Ranked among the leading partners in Pharma/Life Sciences: Regulatory by Chambers France 2026, recognized as a “Next Generation Partner” in France by The Legal 500 EMEA 2026 in Healthcare & Life Sciences, as well as among the best lawyers in Life Sciences by Who’s Who Legal 2025, Sophie Pelé has substantial experience in clinical trial, development, manufacturing and promotion agreements, licensing and distribution schemes, market access transparency, lifecycle management, and hospital-related public procurement.

Time: 
16:10pm - 16:55pm
Agenda Track No.: 
Track 2
Session Type: 
General Session (Presentation)
Force Inline Description: 
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