Regulatory Affairs Expert Witnesses in District of Columbia

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Regulatory Affairs expert witnesses practice in a variety of fields, including pharmaceuticals, medical devices, biotechnology, food safety, and environmental regulations. Some of the most common specialties among Regulatory Affairs expert witnesses include clinical trials regulation, drug approval processes, FDA compliance, product labeling regulations, and quality assurance. They can opine on the effects of regulatory violations, non-compliance penalties, product recalls, adverse event reporting, and regulatory strategy development.

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Mr Steven David SilvermanView profile

ID: 6743128

Mr. Steven Silverman, JD

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Maryland

Mr. Steven D. Silverman has 31 years of experience in Healthcare Regulatory and Compliance. He earned his BA from the University of Michigan and his JD from the University of Pennsylvania Carey Law School. Today, this expert is licensed as an Admission to Practice Law in the District of Columbia. Formerly, this expert served as the Director of the Center for Devices and Radiological Health of the...

FCC & Communications Law Expert WitnessView profile

E-074631

FCC & Communications Law Expert Witness

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New Hampshire

This expert regularly counsels clients on regulatory, transactional and legislative issues affecting the broadcasting, wireless and wireline industries. He is an active member of the Federal Communications Bar Association, for which he has served on the Executive Board since 2013. He also authors a monthly column in Radio Magazine, is editor of a telecom blog, and speaks regularly on panels,...

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Ms Katherine C NorrisView profile

ID: 6220515

Ms. Katherine Norris, MPA

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Hawaii

Ms. Katherine C. Norris has 20 years of experience in the fields of Life Sciences and Corporate Compliance. She earned her BA in Telecommunications and Film from the University of Alabama, and her MPA in Public Policy and Law from the University of Tennessee Knoxville. Formerly, this expert served as the Senior Director of the Compliance and Integrity Programs at NSF Health Sciences, as the...

Ms Margaret E. Guerin-CalvertView profile

ID: 382206

Ms. Margaret Guerin-Calvert, MPA

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District Columbia

Ms. Margaret E. Guerin Calvert has specialized experience in the fields of Business & Finance: Economics, Healthcare: Leadership and Operations, Healthcare: Regulatory & Compliance. They earned their MPA from Princeton University. Formerly, they held roles such as President and a Founding Director at Competition Policy Associates, Inc.. Currently, they work as a Senior Managing Director and...

Regulatory Affairs Expert Witness FAQs

A Regulatory Affairs expert witness provides insight and testimony on matters related to regulatory compliance, product approval processes, and industry standards in various sectors.

These experts are crucial in cases involving pharmaceuticals, medical devices, food safety, environmental regulations, and any sector where regulatory compliance is key.

They can provide insights into FDA approval processes, drug safety regulations, labeling requirements, and other aspects of pharmaceutical regulatory affairs.

Yes, some experts may specialize in specific areas like pharmaceuticals, medical devices, biotechnology, or environmental regulations depending on their experience.

Industry-specific knowledge ensures the expert is familiar with the unique regulatory landscape of that sector, providing accurate and relevant testimony.

Expert Institute offers a personalized approach to help you find the highest quality experts. We source actively-practicing professionals who match all your requirements for specialty areas, work experience, litigation history, fee range, certifications, location, and more.

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