Biomedical Engineering Expert Witnesses in Texas

The SEAK Expert Witness Directory contains a comprehensive list of biomedical engineering expert witnesses who testify, consult and provide litigation support on biomedical engineering and related issues. Biomedical engineering expert witnesses and consultants on this page may form expert opinions, draft expert witness reports, and provide expert witness testimony at deposition and trial. The issues and subjects these biomedical engineering expert witnesses testify regarding may include: 483 Warning Letters, Cardiology, Dental, Fda Approvals, Fda Regulatory Compliance, General Hospital, General Surgical Equipment, Gynecology/Obstetrics, In Vitro Diagnostics, Neurology, Non Active Implants, Ophthalmology, Orthopedic, Prosthetics, and Software.

Medical Devices
  • Biomedical Engineering
  • Patents &Intellectual Property
  • Clinical and Regulatory
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Denise S. Holliday

Medical Device Quality and FDA Regulatory Expert

Capwell Consulting Group LLC

Frisco, Texas
Medical Devices, Biomedical Engineering - Ophthalmology, Spinal Implants, Non-Active Implants, Cardiology, Ventilators, General Hospital, Orthopedic, Gynecology/Obstetrics, General Surgical Equipment, In-Vitro Diagnostics, Dental, Software, Neurology, Prosthetics, Sterilization, 483 Warning Letters, FDA Regulatory Compliance, FDA Approvals
Denise Holliday is a proven strategic innovator and tactical leader in highly regulated environments, including quality management systems, international regulatory compliance, and medical device risk management. As a leading medical device regulatory consultant for Capwell Consulting Group, she provides strategic support to medical technology businesses, healthcare organizations, and startups. She delivers expert testimony for medical device litigation, guiding attorneys and organizations through the complexities of the global medical device industry. Manufacturers and attorneys trust Ms. Holliday to help navigate the complex regulatory landscape of medical device manufacturing and ensure compliance with standards and guidelines. Spanning almost two decades, Ms. Holliday’s career in medical device regulatory compliance and quality assurance showcases her extensive leadership experience. She conducts ISO 13485Medical Device and ISO 9001Quality Management certification audits, spear...
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