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Cahn Litigation Services has completed numerous searches for FDA expert witnesses, providing candidates for each case to the specifications provided by the law firm. In addition, clients may seek an FDA expert for pre-litigation consulting work. Litigation support by an FDA expert witness could include an expert report, expert opinion, depositions, and trial testimony. The FDA Adverse Event Reporting System Database (AERS or FAERS) tracks drug safety the database collects adverse effects reports, medication error reports and product quality complaints. With FDA compliance and good manufacturing practices ( GMP ), companies adhere to minimum quality systems requirements to assure that their products are consistently safe and high in quality. The FDA oversees drugs, food, medical devices, radiation-emitting products, vaccines, biologics, animal and veterinary products, cosmetics, and tobacco products. The US Food and Drug Administration () is responsible for protecting public health by quality control and supervision of a wide range of products. In a high-profile case, or litigation involving a significant financial stake, a law firm may request a subject matter expert with prior expert testimony experience. An FDA expert witness should feel comfortable explaining technology, processes, and procedures to a judge and jury. FDA expert witness candidates typically have a PhD, and years of experience in healthcare, drug development, food and drug safety, pharmacology, FDA regulation, and/or regulatory affairs.