Zantac Expert Witnesses in West Virginia

This expert is a board certified doctor in internal medicine and gastroenterology. He practices at a major medical center. He has been the director of gastroenterology clinics and is a tenured professor of medicine at a major university. He is highly respected in his field.

This highly qualified and board certified expert has over 25 years of experience as a gastroenterologist. He received a B.A. in Biology from the prestigious Dartmouth College and a M.D. from the Uniformed Services University of the Health Sciences and finished a fellowship in Gastroenterology at the US Naval Hospital. A member of both the American Society of Gastrointestinal Endoscopy and the American College of Gastroenterology, he has published and presented extensively on endoscopic procedures. Previously Director of Gastrointestinal Endoscopy at the Fox Chase Cancer Center, he is currently Professor and Chief of Gastroenterology at a major medical university.

This accomplished expert is a highly experienced pathologist who completed medical school in India and went on to complete a residency in Pathology at The University of Pittsburgh School of Medicine. The expert has examined about 25000 liver, kidney and gastrointestinal biopsies in his career.He has been invited to speak over 200 times on topics ranging from hepatitis C, diseases of the kidney, and viral infections in transplant patients.internal fluid illnesses following organ transplants to viral infections. He is experienced in writing reports and testifying for medicolegal cases.

This highly qualified and fellowship trained expert earned his BA from Southern Illinois and his MD from University of Iowa College of Medicine. After his internal medicine residency, this expert pursued a fellowship in gastroenterology at Ohio State University. He has gained over 15 years of experience after serving as a staff physician at several major hospitals as well as a private practice. Formerly, he also served as Medical Director of Endoscopy and Gastroenterology Division Chief at Creighton University Medical Center. This expert remains active in his field as a member of several medical societies including The American Gastroenterological Association. In addition, he as proven himself as a strong research contributor by publishing over 20 journal articles and one textbook chapter. Currently, this expert serves as Clinical Associate Professor of Gastroenterology at a major medical school in the Midwest.

This highly qualified, board certified expert earned his Bachelor's and medical degree from Tufts University. This was followed by an internship and residency in general surgery at the Philadelphia General Hospital. Right after he completed his formal medical education, this expert served in the United States Army and was stationed at Fort Jackson. This expert is a member of numerous medical societies and has received numerous awards for his contributions to the field of medicine. This expert has authored 6 peer reviewed papers and 2 abstracts. This expert previously held numerous positions at various Ivy League University hospital centers, which include attending surgeon, clinical instructor, director of student surgery, clinical instructor, clinical assistant professor, and coordinator of student affairs. This expert currently holds numerous positions at an Ivy League University hospital center, which include clinical professor of surgery, clinical improvement committee, and sits on the board of directors.

A 17-year veteran of the U.S. Food and Drug Administration (FDA), this expert served as the Regulatory Counsel to the Associate Commissioner for Regulatory Affairs, and previously, in scientific, inspectional, compliance and criminal and civil enforcement capacities as an FDA Consumer Safety Officer (CSO), Compliance Officer (CO), a Senior Special Agent (SA) with the Office of Criminal Investigations (OCI) and as an analytical regulatory microbiologist. During his last three years at FDA he spearheaded the agency's integration efforts with Customs and USDA on crosscutting interagency enforcement and operational issues; served as the FDA's point-person in managing the intersection of imports and FDA's new bioterrorism regulations; established joint agency and industry working groups to evaluate counterfeiting and tampering risks to food and drug distribution supply chains; was the agency lead in its strategic planning efforts to reinvent the FDA's import programs; wrote the initial statement of work and acted as program manager over the FDA's new PREDICT, risk-based electronic entry screening system; and directed the development of the FDA's agency-wide Risk-based Import Strategic Plan designed to improve compliance of foods, dietary supplements, drugs, medical devices, cosmetics, and biological products imported into the U.S. As CEO of a FDA consulting firm and Founder of an affiliated law firm, he currently represents domestic and foreign companies of all sizes, assisting them in identifying USDA, FDA, Federal Trade Commission (FTC), Environmental Protection Agency (EPA), and state requirements. He focuses his practice on FDA matters, including but not limited to: matters relating to FDA inspections, FDA criminal, regulatory and administrative enforcement actions for medical devices, drugs, cosmetics, alcohol, tobacco, dietary supplements, and foods.

This extremely qualified clinical expert is an internationally recognized clinical pharmacist, author, patient advocate, and expert in patient adherence with medications and the development of multi-component patient education programs that increase patient adherence from worldwide clinical trials through product launch through post-marketing stages and increase patient safety. She has expertise in the translation of complicated medical terminology into language the average consumer will understand, integration of behavior modification and design, working with medical teams to provide documentation required for FDA approval process, and developing health professional’s tools for patient counseling to ensure that the patient education materials are used correctly. She also has expertise in working with medical device companies and packaging companies to ensure that it will be easy for patients to understand the “how to use” instructions and use the products correctly. She received her BSP degree and completed her residency training in hospital pharmacy at the University of Saskatchewan before receiving her Pharm.D. degree from the University of Cincinnati. She is a founding member of the American College of Clinical Pharmacy, a former member of the Board of Directors and Chairperson of the Business Council at the National Council on Patient Information and Education, and is active in many professional and consumer organizations, including the American Association of Colleges of Pharmacy and the Alliance for Safe Online Pharmacies. She has published 150+ peer-reviewed journal articles on patient education and adherence and serves as a reviewer for the American Pharmacists Association. She is the author of 23 books on how to use medications safety for health professionals and consumers. She has appeared on many radio and television shows to help consumers learn how to take their medications correctly. She is also the former director of clinical affairs at the American Pharmacists Association, which honored her with its Foundation Pinnacle Award for her outstanding leadership. Additionally, she is the former coordinator of the ambulatory patient pharmacy at Sunnybrook Medical Center and a former associate professor of clinical pharmacy at the University of Toronto. Currently, she is the CEO of a major patient education company that develops information to help patients understand how to manage their medications, medical devices and therapies correctly, consults with pharmaceutical companies on how to promote patient understanding and patient safety, develops multi-component patient education programs requiring FDA approval, and develops patient education programs for world-wide clinical trials to increase patient adherence so that the approved FDA dosage is more accurate and thus safer.

This clinical development and regulatory expert has an M.S and Ph.D. in Pharmacology & Toxicology from West Virginia University. A member of the American Society of Clinical Pharmacology & Therapeutics, he has extensive product development experience in the pharmaceutical field. The expert spent his early career in clinical research roles, including a position as the Director of Clinical Research Operations for Univax Biologics. He has since founded/run a biotech development business and acts as both a Professor and Consultant in his field.

This highly qualified expert has 36 years of experience as a practicing gastroenterologist. He received his BA from Antioch College and his MD degree from Rutgers New Jersey Medical School before completing an internal medicine residency at Rush Presbyterian-St. Luke's Medical Center. He completed his gastroenterology fellowship at the Hospital of the University of Pennsylvania. This expert is board certified in internal medicine and gastroenterology. He is active in his field and is a member of multiple gastroenterology societies. He has a research background and has authored several journal articles and has presented at national meetings. He has held academic appointments at several prestigious medical schools including the University of Pennsylvania School of Medicine and Jefferson Medical College. He has received numerous awards during medical school, fellowship and private practice. This expert recently retired from a busy clinical practice and is now working as a consultant.