Clinical Trials Expert Witnesses

San Francisco, California

Pharmacist, Pharmacology- Clinical - medication safety, pharmacology, pharmacokinetics, dispensing, toxicity, anticoagulation, emergency medicine, drug patent, drug labeling, drug administration, clinical pharmacy, pharmacy operations, opioids, adverse drug events, critical care, intensive care unit, resuscitation, clinical trials

Dr. Zlatan Coralic is a full-time practicing Emergency Medicine Clinical Pharmacist at the University of California San Francisco (UCSF) and a Board Certified Pharmacotherapy Specialist. He is also a Clinical Professor in the UCSF School of Pharmacy and in the Department of Emergency Medicine where he provides didactic and experiential training to pharmacy and medical students and residents. Dr. Coralic has published numerous peer-reviewed studies and book chapters. His research focuses on medication safety and efficacy and he has been involved in large multicenter clinical trials. Dr. Coralic is a frequently invited speaker at medical and pharmacy conferences. Dr. Coralic’s most recent expert witness work has been at the state and federal levels. He has provided reviews, opinions, depositions, and testimony in areas of standards of pharmacy care, medication safety, adverse drug events, and patent infringement.

Chicago, Illinois

Pharmacology- Clinical, Pharmacist - Medication, Error, Toxicology, Adverse Drug, Pharmacology, Clinical Trials, Pharmacy, Critical Care, Intensive Care Unit, Prescription, Prevention, Operating Room Medication Safety

Specialization of pharmacology and toxicology of medications utilized both in the hospital and retail pharmacy settings. Detailed analysis of medication errors, adverse drug reactions, and providing strategies for prevention. Particular focus on practice of pharmacy, medication side effects, and medication safety.

Baltimore, Maryland

Pharmaceutical Regulation, Infectious Diseases - Food and Drug Administration (FDA), drug/biologics safety/labeling/post-marketing surveillance, FDA drug/biologics regulations/procedures/applications (INDs/NDAs/BLAs), clinical trials, drug development, pharmacy compounding, HIV, MRSA, antibiotics, hepatitis, osteomyelitis, influenza, C. difficile

Dr. Ross is a Yale fellowship-trained, board-certified infectious disease physician. An active clinician in practice for over 25 years, he provides patient care in the areas of infectious disease and primary care. Dr. Ross holds a medical degree from New York University School of Medicine, and an undergraduate degree in Molecular Biophysics and Biochemistry from Yale University. He completed his internal medicine residency training at NYU Medical Center, and infectious disease fellowship training at Yale University. Dr. Ross also holds a M.S. and Ph.D. in Biochemistry from NYU, and a Master’s Degree in Biomedical Informatics from Oregon Health and Sciences University. Dr. Ross spent 10 years with the FDA’s Center of Drug Evaluation and Review (CDER) as a medical officer, senior medical reviewer, medical team leader, and new drug review office management official. He has extremely broad experience with FDA regulatory submissions (INDs, NDAs, BLAs, post-marketing safety, labeling ...

Milford, New York

Oncology, Hematology - Oncology research, clinical trials

I have 22 years experience practicing medical oncology with current active board certification and 21 years of experience conducting cancer clinical trials, with a leadership role at the Bassett Cancer Treatment Center in Cooperstown NY. I have been honored for excellence in teaching residents and medical students. I have extensive experience with chemotherapy, immunotherapy and targeted therapy administration and side effect management. I am qualified to perform both plaintiff and defense work.

Lovettsville, Virginia

Pharmaceutical Research, Infectious Diseases - pharmaceutical regulation, FDA, drug development, antimicrobials, antiseptics, disinfectants, clinical trials, post-marketing surveillance, drug labels, biologics, medical devices, microbiology, biochemistry, molecular biology, food poisoning, data fraud, biological defense, dairy micro, IP

25 years of experience in infectious disease including food microbiology, chemical/ biological defense and regulatory science. Initial employment in the Federal Government was with the Agricultural Research Service (ARS) performing genetic engineering of dairy bacteria. From there, he went to the Department of Defense, specifically Naval Surface Warfare Center (NSWC), working in chemical and biological warfare defense. Spent 12 years as a Clinical Microbiology reviewer in the Center of Drug Evaluation and Review (CDER) at FDA. He has extensive experience with FDA submissions including: pre-IND, IND, NDA, labeling supplements, and post-marketing for antibiotics, topical antiseptics, biologics and generic drugs. As an independent consultant, provided guidance on microbiology and regulatory affairs for clients developing antimicrobials, medical devices and biologics allowing clients to navigate through the FDA regulatory process. This guidance included providing advice for deve...