FDA Regulations Expert Witnesses in Iowa

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

FDA regulations expert witnesses practice in a variety of fields, including pharmaceutical development, medical devices, food safety, labeling, and clinical trials. Some of the most common specialties include FDA compliance, regulatory submissions, good manufacturing practices, and post market surveillance. They can opine on the effects of regulatory violations, product approvals, warning letters, recalls, and enforcement actions in litigation.

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Average FDA Regulations Expert Witnesses Court Fees

$450/hr

Review Fee

$525/hr

Deposition Fee

$550/hr

Court Fee

Find FDA Regulations Expert Witnesses in nearby states

  • Review Fee $500/hr
    Deposition Fee $500/hr
    Court Fee $500/hr

    This expert is the president of a healthcare government relations and regulatory policy consultancy firm that she founded after an extensive career in healthcare and government. She was the Vice President for Government Relations and Public Policy at Celgene and was the Vice President for Regulatory Policy at GE Healthcare. She served in the administration of President George H.W. Bush as Special Assistant for Legislative and Public Affairs in the Office of the Commissioner, US Food and Drug Administration. She is a certified Regulatory Affairs specialist and is the author of numerous reports and is currently on the Board of Directors of the FDA Alumni Association. Her formal education includes a BA in Government from Georgetown University and an MS in Science and Technology Commercialization from The University of Texas at Austin.

    President, A Biotech Consultancy

    Master of Science (MS), University of Texas at Austin

    Milwaukee,

    Wisconsin

    View profile
  • Review Fee $500/hr
    Deposition Fee $750/hr
    Court Fee $750/hr

    This highly qualified expert has more than 25 years of experience in FDA regulation of medical devices, encompassing nearly all FDA field positions. He earned his BA in biological sciences at California State University and completed MBA courses with Golden Gate University. This expert is certified in regulatory affairs and is an active member of the Regulatory Affairs Professionals Society, the American Society for Quality, and the FDA Alumni Association. Further, he has several publications and has presented both nationally and internationally on topics in his field. In his early career, this expert served as a consumer safety officer, consumer affairs officer, and representative for small businesses at the FDA. He then held several industry leadership roles, including manager of regulatory affairs at Unitek Corporation and vice president of regulatory affairs in clinical research and quality assurance at both Retroperfusion Systems Inc. and Baxter Healthcare Corporation. Additionally, this expert was a medical device specialist, a compliance officer, and the director of import operations at the FDA Los Angeles District as well as a supervisory investigator at the FDA Saint Louis Office. Currently, he is a private consultant for FDA regulated businesses in Illinois.

    Consultant, A private consultancy for FDA regulated businesses in IL

    Bachelor of Arts (BA), California State University

    East Alton,

    Illinois

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Related Specialties

What Can a FDA Regulations Expert Witness Opine On?

New Drug Application (NDA)

Process for seeking FDA approval of drugs.

Investigational New Drug (IND) Application

Request to begin clinical trials on drugs.

Biologics License Application (BLA)

Application for approval of biological products.

Abbreviated New Drug Application (ANDA)

Application for generic drug approval.

Food Facility Registration

Registration of food manufacturing facilities.

Labeling Compliance Review

Evaluation of product labeling for compliance.

FAQs for Fda Regulations Expert Witnesses

What is a fda regulations expert witness?

An FDA regulations expert witness is a specialist who explains how FDA laws and compliance standards apply to a case. They assist by reviewing records, preparing opinions, testifying, and clarifying regulatory issues.

What types of cases may benefit from the expertise of an FDA Regulations expert witness?

An FDA regulations expert witness handles cases involving drug and device approvals, labeling, advertising, clinical trials, GMP compliance, recalls, and regulatory enforcement.

How can an FDA-regulations expert witness strengthen regulatory causation arguments?

An FDA-regulations expert witness strengthens regulatory causation arguments by linking specific FDA standards, compliance gaps, and regulatory history directly to the alleged harm.

What qualifications should counsel prioritize when selecting an FDA-regulations expert witness?

Counsel should prioritize an FDA-regulations expert witness with direct FDA or industry experience, advanced regulatory credentials, case-testifying history, and strong scientific or legal training.

How does an FDA-regulations expert witness evaluate compliance with labeling requirements?

An FDA-regulations expert witness evaluates labeling compliance by comparing product labels to FDA statutes, regulations, guidance, and enforcement history to identify gaps or violations.

What is Expert Institute’s process for selecting fda regulations 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.

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