Experience

Experience across litigation support, governance, transactions, and regulated medical technology, with a focus on judgment, risk, and decision-making in complex environments.

Litigation & Dispute-Related Experience

Experience includes litigation support and expert analysis in matters involving regulated medical technology and complex product issues.

Expert witness and consulting support in disputes involving regulated medical devices
Technical analysis related to product performance, design controls, and risk management
Support for discovery preparation, interrogatory development, and technical issue framing
Participation in on-site inspections and technical evaluations, in coordination with counsel
Matters involving product liability, IP and trade secrets, unfair competition, warranty claims, and transaction-related disputes

Transactions & Strategic Alternatives

Transaction experience includes diligence and advisory support for medical device companies operating in regulated environments.

Buy-side and sell-side diligence support for medical technology transactions
Advisory support during strategic alternatives, restructuring, and corporate transitions
Assessment of product, regulatory, and quality-system risk in transaction contexts
Support for boards and executives during transaction decision-making

Governance & Board Leadership

Governance experience includes board leadership, risk oversight, and fiduciary responsibility across private and non-profit organizations.

Independent board service and advisory roles for medical technology companies
Board leadership in non-profit and private-company settings
Governance restructuring, executive transition, and financial oversight
Fiduciary decision-making during periods of organizational stress

Product & Regulatory Complexity

Experience spans product development, commercialization, and regulatory remediation of regulated medical technologies, including surgical robotics systems.

Experience across the full lifecycle of regulated medical devices
Product development, design controls, and commercialization in regulated environments
FDA enforcement / remediation experience
Interface between engineering, marketing, clinical use, quality systems, and regulatory requirements
Market and commercialization decisions grounded in product realities

For details on how this experience informs governance, independence, and engagement discipline, see Governance.