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Abstract Structure

Conference on Life Sciences and Healthcare: Legal, Ethical & Regulatory Pathways for GCs

Mumbai / 07 November 2025

BRIEF

India's healthcare, pharma, life sciences, and medical devices industries are undergoing rapid transformation, spurred by innovation, regulatory change, digital disruption, and increasing global scrutiny. In this high-stakes environment, General Counsels (GCs) are playing a pivotal role, not just as risk managers, but as strategic advisors navigating the intersection of law, ethics, compliance, innovation, and business continuity.

This conference is designed specifically for GCs and senior legal leaders from across the healthcare spectrum, covering pharmaceuticals, biotechnology, life sciences R&D, hospital networks, medtech manufacturing, diagnostics, and digital health platforms. The goal is to foster practical dialogue on the evolving regulatory environment, corporate governance, cross-border risk, IP strategy, internal investigations, ESG mandates, and emerging technologies.

OBJECTIVES

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  • Provide a platform for peer-to-peer learning among legal leaders in the healthcare space

  • Discuss high-impact regulatory and compliance trends affecting the industry

  • Address challenges in internal investigations, whistleblower protection, and ethics management

  • Share insights into strategic IP protection and licensing in a globalised R&D context

  • Understand the GC’s evolving role in cross-border operations, ESG, and risk leadership

TARGET AUDIENCE

  • General Counsels & Heads of Legal

  • Senior Legal Counsels, Chief Compliance Officers

  • Regulatory Affairs Heads

  • Chief Compliance Officers

  • Company Secretary

  • Chief Financial Officers

AGENDA (tenative - to be finalised)

  • Recalibrating Risk: Role of GC in the Healthcare Boardroom

  • Ethics, Whistleblowing & Internal Investigations: Raising the Bar

  • M&A in Healthcare: Navigating Regulatory & Cultural Integration

  • AI, Digital Health & Data Privacy: What Should GCs Be Watching?

  • Anti-bribery and Anti-corruption Risks in Pharma Marketing and Clinical Research

  • Advertising, Labeling and Marketing of Drugs & Medical Devices

  • Managing Legal Risks in Cross-Border Supply Chains

  • Best Practices for Joint Ventures and Collaborations in R&D and Manufacturing

  • Sustainable Manufacturing and Green Compliance in Pharma and MedTech

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