FDA Approval Expert Witnesses in South Carolina

We’ll help you retain an industry-leading FDA Approval expert

FDA approval expert witnesses practice in a variety of fields, including regulatory affairs, clinical research, pharmaceuticals, and medical devices. Some of the most common specialties include FDA compliance, drug development, labeling, and post-market surveillance. They can opine on the effects of FDA regulations, approval pathways, safety standards, and enforcement actions on products and companies.

Find an expert witness near you

Select your state

What party are you representing?

Average FDA Approval Expert Witnesses Court Fees

Review Fee

Deposition Fee

Court Fee

Find FDA Approval Expert Witnesses in nearby states

  • Review Fee $250/hr
    Deposition Fee $250/hr

    This certified compounding pharmacist has received his training from a top pharmacy program and holds clinical and academic positions in his field at both pharmacy and medical schools. He has given invited lectures on compounding pharmacy, and has authored major publications on the topic. Furthermore, he has been in practice since 1977 and has owned a compounding-only pharmacy since 2003. He serves on the North Carolina Board of Pharmacy and the USP Compounding Expert Committee for the 2010-2015 cycle. Memberships include the American Society for Pharmacy Law and the National Associations of Boards of Pharmacy.

    Clinical Associate Professor, A major pharmacy college

    Master of Science (MS), University of North Carolina, Chapel Hill

    Hickory,

    North Carolina

    View profile
  • Review Fee $250/hr
    Deposition Fee $500/hr
    Court Fee $500/hr

    This expert has over 40 years of experience in the Pharmaceutical and Pharmaceutical Packaging industries. He has published five books and has instructed professionals at the graduate level in Quality Assurance and Regulatory Affairs at a major university's pharmacy school. As a former Director of the Science Branch of the Philadelphia District FDA, he directed a laboratory staff of 30 in methods verification of New Drug Applications and Abbreviated New Drug Applications, Drug Product Surveys, and Research Projects. Currently, this expert is an independent consultant in which he assists pharmaceutical firms in technical, regulatory, and management areas to ensure their clients' products hit the market in a timely manner. He assists attorneys as an Expert Witness/Subject Matter Expert in Pharmaceutical cases.

    Founder/Principal, A consulting services for pharmaceutical firms

    Master of Business Administration (MBA), Temple University

    Savannah,

    Georgia

    View profile
  • This expert's professional career has spanned 50 years, while for the past 20 years he has specialized in guiding companies through the CE marking process for products prepared to enter the EU market and for companies in the US who want CE marking on their products for market flexibility and/or liability protection, many of which are medical devices and machinery. This expert conducts forensic legal analysis of companies' Quality Management Systems (ISO 9001), Environmental Management Systems (ISO 14001), and Quality System Regulations as stipulated by the FDA. He has hosted over 450 seminars and workshops and has published more than 300 articles and multiple books in the areas of Liability, EU Directives/CE Marking, Technical Standards, FDA Quality System Regulations, and ISO 90001 and 14001. He has developed and delivered on-site training programs on product liability exposure for medical device insurance companies, as well as for corporate counsel, defense counsel, and trial attorneys involved with medical devices and medical device manufacturers. As a Senior Consultant for both Excel Partnerships and SAI Global, he also developed and delivered on-site training programs on CE marking for the Medical Devices Directive and related Quality Management Systems. As Legal Expert/Expert Witness he has prepared legal materials for use in litigation involving Quality Systems and CE marked products as well as EU Administrative Reviews.

    Legal Consultant and President, International Standards and Regulations Consulting Firm

    Doctor of Philosophy (PhD), University of Kansas

    Marietta,

    Georgia

    View profile
  • Review Fee $400/hr
    Deposition Fee $400/hr
    Court Fee $400/hr

    This expert has more than a decade of experience in pharmacy practice and pharmaceutical marketing. He earned his PhD in pharmacy care administration from the University of Georgia following a BS in pharmacy from Ohio Northern University. The expert is certified in pharmacy-based immunization delivery and is a member of numerous professional societies. He previously served as pharmacist for Rite Aid and as an assistant professor of pharmacy administration at the Georgia Campus School of Pharmacy. The expert currently serves as an associate professor of pharmacy administration at a GA medical school.

    Administrator, A Major Medical School in GA

    Doctor of Philosophy (PhD), University of Georgia

    Winder,

    Georgia

    View profile
  • Review Fee $325/hr
    Deposition Fee $425/hr
    Court Fee $425/hr

    This highly-qualified expert has over 15 years of experience as a pharmacist dealing with issues like medication safety, medication errors, and medication policy. She earned her PharmD from the University of North Carolina before completing a drug information specialty residency at Thomas Jefferson University Hospital. This expert is a licensed pharmacist in North Carolina and is certified by the American Heart Association in basic life support. She is active in her field as a member of the American Society of Health-System Pharmacists, a researcher on several pharmacy research studies, an author of multiple pharmacy publications, and a speaker at several industry conferences throughout her career. She has formerly served as a clinical instructor at the University of the Sciences in Philadelphia, a clinical pharmacist in the ambulatory setting at the Duke Outpatient Clinic, and a clinical pharmacist in medication safety at Duke University Medical Center. This expert currently serves as a clinical pharmacist for drug information at a university-affiliated medical center and as the preceptor for the drug information rotation at two North Carolina universities.

    Clinical Pharmacist, Drug Information, A University-Affiliated Medical Center in NC

    Doctor of Pharmacy (PharmD), University of North Carolina

    Durham,

    North Carolina

    View profile
  • Review Fee $275/hr
    Deposition Fee $350/hr
    Court Fee $350/hr

    This highly-qualified pharmacist earned her PharmD at the University of Georgia and is a licensed pharmacist in the state of Georgia. Her work focuses on ambulatory care pharmacy, as well as transitions of care, patient education, cardiology, diabetes, and COPD. She is active in her field as a member of the American College of Clinical Pharmacy and the American Society of Health System Pharmacists. She has formerly served as a pharmacist at Atlanta Veterans Affairs Medical Center, Athens Veterans Affairs Community Outpatient Clinic and Mercy Health Center. This expert currently serves as a clinical associate professor at a college of pharmacy and as an ambulatory care clinical pharmacist at a major medical center in Georgia.

    Clinical Associate Professor, A University in GA

    Doctor of Pharmacy (PharmD), University of Georgia

    Tucker,

    Georgia

    View profile

What Can a FDA Approval Expert Witness Opine On?

Preclinical Testing

Assess safety and efficacy in labs.

Investigational New Drug Application

Submit data for human trial approval.

Phase 1 Clinical Trials

Test drug on a small group of subjects.

Phase 2 Clinical Trials

Evaluate effectiveness in larger patient groups.

Phase 3 Clinical Trials

Confirm effectiveness through extensive testing.

New Drug Application Submission

Request approval for market release.

FAQs for Fda Approval Expert Witnesses

What is a fda approval expert witness?

An FDA approval expert witness is a specialist who explains FDA rules and drug or device approval processes in legal cases. They assist by reviewing records, offering opinions, and testifying to clarify FDA compliance issues.

What types of cases may benefit from the insights of an FDA Approval expert witness?

An FDA approval expert witness supports drug, device, biologic, clinical trial, labeling, marketing, compliance, and product liability cases involving FDA regulatory standards.

How can an FDA Approval expert witness evaluate regulatory compliance timelines?

An FDA approval expert witness evaluates regulatory compliance timelines by comparing documented development, submission, and review milestones against FDA guidance and statutory deadlines.

What qualifications should an FDA Approval expert witness possess for complex litigation?

An FDA approval expert witness should have advanced scientific or medical training, regulatory experience, and a proven track record with FDA approval processes and complex litigation.

How does an FDA Approval expert witness assess adequacy of premarket submissions?

An FDA approval expert witness assesses adequacy of premarket submissions by comparing study design, data quality, and labeling to current FDA regulations, guidance, and review standards.

What is Expert Institute’s process for selecting fda approval expert witnesses?

Expert Institute delivers a tailored approach to connect you with top-tier experts. We identify actively practicing professionals who meet your exact criteria for specialty, experience, litigation background, fee structure, credentials, location, and more.

Connect with the Fda Approval expert witness you need to win your case

Representing*
Close Icon

Your information will not be shared. View our privacy policy.