Found 20 regulatory affairs Experts and Expert Witnesses.
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| Over 35 years experience of trial experience, Biomedical Science, Toxicology and Regulatory Compliance for Drugs, Biologics, Diagnostics and Pesticides. Well-versed in Drug and Medical Product Development, licensing, patents and acquisitions....
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| 44 years experience in securities investments.
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| 30+ years bank executive experience, plus 13 years litigation support consulting for plaintiff and defense in over 500 cases. No geographic restrictions.
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| Ph.D Purdue University Electrical Engineering, telecommunications & wireless technologies; cellular, PCS, GSM, Wi-Fi, WiMax, Bluetooth etc. Expert witness in many cases; laboratory tests, expert reports, infringement and validity analysis, depositions, courtroom testimony....
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| Expert on FDA matters and quality, regulatory and production issues for drugs, biologics and devices
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| Providing unique perspectives and practical assistance in drug issues based on 37 years with FDA in all aspects of drug regulation and on consulting and expert witness experience.
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| EW #1082 is a certified toxicologist (Diplomate of the American Board of Toxicology)
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| Experienced pharmaceutical scientist able to assist in litigation involving scientific evidence as well as patents and trademarks to include evaluation of science issues relevant to business mergers.
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| Toxicology expert.
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| EW #367 is currently in his twentieth year of evaluating drug and chemical adverse health effects cases for causation and adequacy of warnings.
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| Pharmacutical industry expert with over 30 years of experience domestically and internationally. Managed the 1st co-promotion arrangement in the industry.
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| Board Certified Toxicologist, Expert on Causation, Occupational and Environmental Toxicology, Technical Management of Mass Toxic Tort Litigation, Medical Evaluation and Health Survey Team
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| PH.D. physical organic chem., 25 years pharma, chem., phys. and bio. analysis, 13 years management of labs., 6 years lab consult. ICH, cGMPs, FDA and DEA regs.- all lab. functions (tech., GMP and RA)
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| EW #13806 has a background as a hospital Medical Director, and has widely evaluated and consulted to hospitals and medical staffs on organizational, quality, and regulatory issues.
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| Professional mariner, 40 yrs experience in the marine industry. Unlimited Tonnage Master. Experienced with injuries, collisions, navigation, seamanship, recreational boat accidents, fishing vessels.
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| Dr. Mayer is an academic epidemiologist and biostatistician trained in medicine, psychiatry and statistics. He divides his time between Baltimore and Phoenix. He has done expert witnessing for 30 years....
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| Data protection, recovery and analisys expert
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| Board Certified Forensic Examiners and Forensic Engineers-Technologists in floor failure analysis, slip, trip and fall causation. Floor covering industry expert in materials and design of remediation.
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| Recognized worldwide premier provider of engineering and management consulting services to the engineering, legal, regulatory, industrial, commercial and construction sectors.
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| Board-certified Gastroenterologist with over 20 years experience. Extensive experience in Medical Record Review and Testimony for Plaintiff and Defense attorneys.
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| Looking for a regulatory affairs expert?
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Find Regulatory Affairs experts and consultants for Regulatory Affairs litigation support at www.expertwitness.com. Available to be Regulatory Affairs expert witnesses and provide Regulatory Affairs forensic consulting in Regulatory Affairs litigation, in addition prepare Regulatory Affairs expert witness reports for use in deposition and/or in-court trial testimony.
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Categories To Find "Regulatory Affairs" Experts:
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MEDICAL DEVICES |
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A medical device is an instrument, apparatus, implement, machine, contrivance, implant, in vitro reagent, or other similar or related article, including a component part, or accessory which is:
recognized in the official National Formulary, or the United States Pharmacopoeia, or any supplement to them,
intended for use in the diagnosis of disease or other conditions, or in the cure, mitigation, treatment, or prevention of disease, in man or other animals, or
intended to affect the structure or any function of the body of man or other animals, and which does not achieve any of its primary intended purposes through chemical action within or on the body of man or other animals and which is not dependent upon being metabolized for the achievement of any of its primary intended purposes.
as defined by the US FDA.
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MERGERS / ACQUISITIONS |
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The phrase mergers and acquisitions or M&A refers to the aspect of corporate finance strategy and management dealing with the merging and acquiring of different companies as well as other assets. Usually mergers occur in a friendly setting where executives from the respective companies participate in a due diligence process to ensure a successful combination of all parts.
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PHARMACY |
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Pharmacy (from the Greek φάρμακον = drug) is the profession charged with ensuring the safe use of medication. Traditionally, pharmacists have compounded and dispensed medications on the orders of physicians. More recently, pharmacy has come to include other services related to patient care including clinical practice, medication review, and drug information. Some of these new pharmaceutical roles are now mandated by law in various legislatures. Pharmacists, therefore, are drug therapy experts, and the primary health professionals who optimize medication management to produce positive health-outcomes.
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Regulatory Affairs Experts Witnesses - Regulatory Affairs Forensic Consultants.
Find Regulatory Affairs experts and consultants for Regulatory Affairs litigation support. Available to be Regulatory Affairs expert witnesses and provide Regulatory Affairs forensic consulting in Regulatory Affairs litigation, in addition prepare Regulatory Affairs expert witness reports for use in deposition and/or in-court trial testimony.
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