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This highly qualified expert received his Masters of Medicine and Surgery from the Seth G S Medical College & KEM Hospital. He then received his Master of Public Health from the Harvard University School of Public Health. He then went on to complete his Residency in Internal Medicine at Case Western Reserve University. He then did fellowships in Gastroenterology at Brown University and Advanced Endoscopy at Case Western Reserve University. This expert is duel board certified in Internal Medicine and Gastroenterology. He has published more than 50 peer reviewed articles in professional journals and is a frequent lecturer at Top Ranked Universities and Hospital Programs. He belongs to multiple professional organization committees including the Gastroenterology Fellowship Committee, the Scientific Program Committee and Guidelines Committee for the American Board of Gastrointestinal Endoscopy . He is currently an Associate clinical Professor at a Top Ranked University.
Attending, A Major TX Medical Center
Master of Business Administration (MBA), University of Dallas
Dallas,
Texas
This expert has successfully aided many national and international medical device companies with on-site help during FDA audits, FDA-483 responses, Warning Letter Responses, Consent Decree Corrections, ISO audits and readiness, developing and implementing compliant quality systems. She is a former FDA Regional Medical Device Expert and currently provides personalized, FDA regulatory and quality solutions and training to both small and large companies, and entrepreneurs. This expert has been invited to speak nationally, and has authored 6 publications in FDA regulatory and quality matters.
FDA Regulation Consultant
Bachelor of Science (BS), University of South Carolina
Dallas,
Texas
This highly-qualified expert has nearly 20 years of experience in the field of gastroenterology. He earned his BA biology from Texas A&M University and his MD from the University of Texas. He subsequently completed an internal medicine residency at the University of Texas and a gastroenterology and hepatology fellowship at the University of Alabama. He completed an additional fellowship in advanced therapeutic endoscopy/ERCP and endoscopic ultrasonography with Drs. Marc Catalano and Joseph Geenen. This expert is board-certified in internal medicine and gastroenterology, and is active in his field as a member of the American Society of Gastrointestinal Endoscopy, the American Gastroenterology Association, and the American College of Gastroenterology. He is also active in his field as an author of numerous peer-reviewed publications. Currently, this expert is the medical director of the GI Lab at a medical center, as well as a faculty member at a medical school and in the gastroenterology fellowship program for a hospital system, all in Texas.
Faculty, A medical school in TX
Doctor of Medicine (MD), University of Texas
Texas
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What Can a Zantac Expert Witness Opine On?
Medication Review
Evaluate patient's current medications.
Patient Counseling
Discuss medication usage and side effects.
Dosage Adjustment
Modify medication dosage as needed.
Drug Interaction Screening
Check for potential drug interactions.
Side Effect Management
Address and manage adverse effects.
Therapeutic Monitoring
Monitor effectiveness of the medication.
FAQs for Zantac Expert Witnesses
What is a zantac expert witness?
A Zantac expert witness is a medical or scientific professional who explains Zantac-related health and causation issues in court. They assist by reviewing medical records, analyzing studies, and testifying to clarify complex Zantac lawsuit claims.
What types of cases may benefit from the testimony of a Zantac expert witness?
A Zantac expert witness supports cancer lawsuits involving NDMA contamination, product liability, failure to warn, medical causation, dosage, labeling, and FDA regulatory compliance.
How can a Zantac expert witness support Daubert admissibility challenges?
A Zantac expert witness supports Daubert admissibility by presenting scientifically reliable methods, data, and reasoning that link Zantac use to alleged injuries.
What specific methodologies does a Zantac expert witness rely upon?
A Zantac expert witness relies on epidemiological studies, toxicology data, FDA records, medical literature, and differential diagnosis to assess NDMA risk and causation.
What credentials should a Zantac expert witness possess for complex product liability matters?
A Zantac expert witness should have medical, pharmacology, or toxicology credentials, litigation experience, and specific research or clinical expertise with ranitidine and NDMA risks.
What is Expert Institute’s process for selecting zantac expert witnesses?
Expert Institute delivers a tailored approach to connect you with top-tier experts. We identify actively practicing professionals who meet your exact criteria for specialty, experience, litigation background, fee structure, credentials, location, and more.