Pharmaceutical

Innovation in the pharmaceutical industry has a widespread impact that ignites competition and drives conflict in one of the most scrutinized areas of life sciences. WIT represents highly credentialed experts who know the pharmaceutical industry and can address issues regarding the research, development, and manufacturing of drugs and medications. 

Pharmaceutical companies face constant challenges, including protecting intellectual property and navigating shifts in government regulations. Drug and vaccine development is rapidly evolving, with scientific advancements and innovative technologies emerging constantly. As a result of this new era of rapid evolution, litigation will likely ensue. WIT represents prominent life sciences experts in the science, research and development, and clinical trial protocols involved in new drugs and vaccines.WIT has been involved in some of the most prominent disputes associated with vaccines and drugs, including dozens of pharmaceutical lawsuits associated with the opioid crisis, the pneumococcal vaccine, the mumps vaccine, and the influenza vaccine.

Pharmaceutical Expert Team

Our pharmaceutical expert team is comprised of world-class academics, industry executives, and former government regulators who were carefully selected for their knowledge, experience, and ability to communicate effectively. The team features:

  • Academics: Leading scholars from top institutions with specialized expertise in immunology, vaccine efficacy and potency, drug development, and regulatory science
  • Industry Executives: Former senior pharmaceutical executives with hands-on experience in product development, clinical trials, regulatory strategy, and corporate transactions
  • Regulators: Ex-government officials and former FDA regulators with deep knowledge of drug approval processes, compliance requirements, and pharmaceutical policy standards

Our Experts

Our focus on the pharmaceutical industry allows us to bring together independent testifying experts under one virtual roof to address issues in complex legal disputes involving:

  • Clinical Trials
    Trial Design, Data Analysis
  • Drug Safety
    Diversion Prevention, Counterfeit Detection
  • Drug Types
    Biologics, Small Molecules, OTC Drugs
  • Industry Landscape
    Market Trends, Regulatory Impact
  • IP and Compliance
    Patent Disputes, Regulatory Adherence
  • Manufacturing
    cGMP, FDA Compliance
  • Marketing and Sales
    Labeling, Pricing Strategies
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