Overview
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Christina is a health sciences attorney focusing on counseling companies on a wide variety of regulatory issues. She also has experience in the defense of companies, including pharmaceutical manufacturers, in civil litigation, risk assessment, and internal and government investigations.

  • Defended pharmaceutical companies in matters concerning investigational new drugs and marketed products, including class actions.
  • Counseled and defended a pharmaceutical company in a grand jury investigation and in matters regarding a failed clinical trial.
  • Defended a multinational chemical company against allegations of its agricultural products causing adverse effects.
  • Conducted internal investigations and risk assessments.
  • Counseled companies on regulatory, competitive, and litigation risks for marketed products.
  • Evaluated promotional claims for prescription drugs, medical devices, and dietary supplements.
  • Advised pharmaceutical companies regarding compliance with FDA and foreign regulations relating to conduct of clinical trials, adverse event reporting and analysis, sales promotion, and marketing practices and materials.
  • Assessed potential litigation risks in published medical literature, proposed protocols, regulatory submissions, informed consent documents, scientific disclosures, and medical letters.
  • Intensive expert witness investigation and development.
  • Prepared witnesses for deposition and trial.
  • Assisted clients with the preparation of SEC filings and conducted due diligence in conjunction with securities offerings and mergers and acquisitions.
  • Counseled clinical laboratories regarding their compliance with the Clinical Laboratory Improvements Amendments of 1988, as well as state clinical laboratory laws and regulations.

Christina is a health sciences attorney focusing on counseling companies on a wide variety of regulatory issues. She also has experience in the defense of companies, including pharmaceutical manufacturers, in civil litigation, risk assessment, and internal and government investigations.

  • Defended pharmaceutical companies in matters concerning investigational new drugs and marketed products, including class actions.
  • Counseled and defended a pharmaceutical company in a grand jury investigation and in matters regarding a failed clinical trial.
  • Defended a multinational chemical company against allegations of its agricultural products causing adverse effects.
  • Conducted internal investigations and risk assessments.
  • Counseled companies on regulatory, competitive, and litigation risks for marketed products.
  • Evaluated promotional claims for prescription drugs, medical devices, and dietary supplements.
  • Advised pharmaceutical companies regarding compliance with FDA and foreign regulations relating to conduct of clinical trials, adverse event reporting and analysis, sales promotion, and marketing practices and materials.
  • Assessed potential litigation risks in published medical literature, proposed protocols, regulatory submissions, informed consent documents, scientific disclosures, and medical letters.
  • Intensive expert witness investigation and development.
  • Prepared witnesses for deposition and trial.
  • Assisted clients with the preparation of SEC filings and conducted due diligence in conjunction with securities offerings and mergers and acquisitions.
  • Counseled clinical laboratories regarding their compliance with the Clinical Laboratory Improvements Amendments of 1988, as well as state clinical laboratory laws and regulations.

Education

  • Villanova University Charles Widger School of Law, J.D., 1994
  • Saint Joseph’s University, B.A., summa cum laude, 1985

Bar Admissions

  • Pennsylvania