New Jersey
This highly-qualified expert has over 25 years of experience as a pharmaceutical and drug delivery executive involved in commercial agreements, new product launches, commercial agreements, product pricing, and clinical trials. He earned his BA in economics from St. Francis College before earning his MBA in finance from New York University. He also stays active in his field as a chartered...
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New Jersey
This Pharmaceutical Business Executive has a proven history of strategic marketing experience and increasing sales growth at Eisai, Roche, and Pfizer, among other firms. He previously served as Director of Marketing, the Head of Primary Care and Speciality Marketing, and the Head of Commercial Operations in the Americas at Eisai. He now serves as a consultant and mentor at the C-suite and Board...
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New Jersey
This expert has over 30 years of experience in family and addiction medicine. After gaining his BS in pharmacy at Temple University School of Pharmacy, his degree in osteopathic medicine at the Philadelphia College of Osteopathic Medicine, and completing his residency in family practice at Underwood Memorial Hospital, he served as a staff physician in family practice at numerous northeastern...
New Jersey
This accomplished senior finance executive has more than 30 years of experience within the global pharmaceuticals, healthcare, pharmacy benefits management and manufacturing industries. Most recently, he held the title of Vice President of Finance, Gross Margin Planning and Strategic Pricing with Express Scripts from April 2013 to March 2016. In this role, he managed the finances, strategic...
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An FDA Approval expert witness provides insight on regulatory compliance, drug approval processes, and medical device clearance. They can testify on whether proper procedures were followed.
Cases involving pharmaceuticals, medical devices, food safety, and cosmetics often require an FDA Approval expert witness. These experts are crucial in product liability or patent infringement cases.
In pharmaceutical litigation, an FDA Approval expert can provide testimony on drug development, clinical trials, labeling requirements, and post-market surveillance to establish if there was any negligence.
Yes, some experts specialize in specific areas like pharmaceuticals, medical devices, biologics, dietary supplements, or food products depending on their experience with FDA regulations.
Regulations and guidelines from the FDA frequently change. An expert with recent industry experience will have up-to-date knowledge about these changes and how they impact your case.
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.