Patel also has experience in product development, project management, partnering, due diligence product and company , auditing GMP, GLP, and GCP , and risk management company strategies.. Carrie Rabe provides consulting services to industry and counsel on a variety of FDA regulated products.
In addition, she has prepared in-depth critical reviews for industry clients on health effects of products that are the subject of regulatory, legal, or public scrutiny. Scarola has experience in drug and device development and regulation in the United States and Europe.
She has assisted in the development of regulatory strategies, as well as the preparation and quality assurance reviews of regulatory submissions in both the United States and Europe. Additionally, she has conducted on-site audits to evaluate the quality of bio analytical and clinical data in accordance with FDA criteria.
She has experience in litigation support in the form of expert witness identification, medical record review, and assisting in the development of scientifically-sound legal strategies.
Daniel Solorio provides regulatory and quality strategic support to clients. He has led high-performance operations teams through both early and late phase development activities, including multiple clinical trial programs, quality and compliance, NDA submissions, product approvals, launches, and post marketing efforts.
Bryce Whited provides consultation in all phases of the development, approval, and marketing of medical devices and combination products.
He has extensive hands-on experience in U. She manages auditor selection, reviews and approves all audit reports, and conducts audits alongside the team. John LoPiccolo has over 31 years of pharmaceutical, biotech, medical device, consumer products, and nutraceutical industry management experience primarily focused on operations and GMP compliance.
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Get directions. Translated into normal English, this says: " We can find scientists with the requisite lack of ethical standards to permit them to trade false information for money. From on, the Washington office was run by Matthew Weinberg , Myron's son. Myron Weinberg and his staff were very substantially responsible for identifying European WhiteCoats secret consultants for Philip Morris, and they established an office in Brussels for this purpose.
However the Scandinavian WhiteCoats were part of a different cluster, made up of friends and associates of the organiser, Torbjorn Malmfors. Congress was investigating the Weinberg Group.
Representative John Dingell Democrat of Michigan said the firm's practices "raise serious issues about whether science is for sale. Some studies have indicated that small amounts of Bisphenol A, which is present in a wide range of plastics, "can disrupt hormone systems in laboratory animals and possibly increase the risk of cancer or other serious illness," reported ABC.
In a April pitch to DuPont , The Weinberg Group proposed an inverted research strategy to help defuse the growing controversy over the health impacts of perfluorooctanoic acid PFOA , a compound used to make Teflon. Terrence Gaffney , wrote, "DuPont must shape the debate at all levels. Gaffney also proposed to "develop 'blue ribbon panels' of thought leaders on issues related to PFOA" and to "coordinate the publishing of white papers on PFOA, junk science and the limits of medical monitoring.
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