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Sidley’s industry-recognized Tier 1 Global Life Science practice leverages integrated teams across regulatory, compliance, enforcement, litigation, corporate, and transactional practice groups to advise life sciences and healthcare clients throughout their lifecycle.

Corporate and Transactional

Licensing and Partnering
M&A
Capital Markets
Private Equity
Emerging Companies and Venture Capital
Restructuring

Regulatory and Compliance

FDA Regulatory and Compliance
Healthcare Regulatory and Compliance
GMP Compliance
Global Drug Pricing
EU Food, Drug and Medical Device Regulatory
FDA and CMS Engagement Strategies
Other Government Engagement Strategies
Clinical Trials and Pharmacovigilance
Privacy and Cybersecurity
SEC Regulatory
Antitrust and Competition
ESG and Sustainability
International Trade, Customs, and Economic Sanctions

Government Investigations and Enforcement

DOJ Civil and Criminal Investigations
FDA Enforcement
FCPA and Anti-Bribery
SEC Enforcement
EU Whistleblower

Litigation

Product Liability and Mass Torts
IP Litigation
False Claims Act Litigation
Administrative and Regulatory Litigation
Shareholder Litigation
Commercial Litigation and Disputes
Global Arbitration, Trade and Advocacy

Life Sciences

Pharmaceutical Drugs and Biologics
Medical Devices and Equipment
Development-Stage Life Sciences Companies
Cell and Gene Therapy
Digital Health and AI Technologies
Wholesalers and Distributors
Contract Manufacturers and Other Supply Chain Participants
gribusiness and Food
Animal Health
Cosmetics
Dietary Supplements and Over-the-Counter (OTC) Products
Medical Foods

Healthcare

Clinical and Molecular Diagnostic Laboratories
Hospitals, Health Systems, Physician Practices, and Specialty Healthcare Providers
Pharmacies
Telehealth and Telemedicine

Contacts