Pharmaceuticals
Our pharmaceutical expert witnesses possess extensive knowledge and experience in drug development, clinical trials, and drug safety. They provide objective and reliable testimony in legal disputes related to pharmaceutical issues, offering valuable insights into product liability claims, patent disputes, and regulatory compliance.
Drug Development
Preclinical studies
Clinical trials
FDA approval
Drug manufacturing
Drug formulation
Intellectual Property
Patents
Trademarks
Copyrights
Trade secrets
Licensing
Regulatory Compliance
FDA regulations
Drug labeling
Advertising and promotion
Good manufacturing practices
Post-market surveillance
Quality Control
Quality management systems
Stability testing
Product testing
Process validation
Batch release
Pharmacovigilance
Adverse event reporting
Risk management
Drug safety monitoring
Signal detection
Post-market surveillance
Medical Affairs
Medical education
Scientific communications
KOL engagement
Medical information
Publication planning
Market Access
Health economics
Outcomes research
Pricing and reimbursement
Market research
Payer negotiations
Supply Chain Management
Inventory management
Logistics
Distribution
Vendor management
Cold chain management
Clinical Research
Study design
Patient recruitment
Data management
Statistical analysis
Trial monitoring
Biotechnology
Gene therapy
Cell therapy
Regenerative medicine
Gene editing
Immuno-oncology