Found 26 fda 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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| MD, PhD. Internationally respected, experienced, published neuropsychiatrist, psychopharmacologist, forensic specialist (civil: plaintiff / defense /objective) & author.
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| CLINIPHARM SERVICES, established in 1988, is a Southern California-based consultancy specializing in all aspects of contemporary pharmacy practice and systems.
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| Objective, accurate expert testimony. Diplomate of the American Board of Forensic Dentistry
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| Expert in Industrial Engineering, Operations/Logistics Management, Automation Systems & Equipment, Material Handling Equipment, and MRP, WMS, DCS, MHS, and TMS Software Integration.
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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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| 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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| Expert on FDA matters and quality, regulatory and production issues for drugs, biologics and devices
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| Qualified as an expert for medical devices and technology. Ph.D. in Biomedical Engineering, Licensed Engineer and Certified Clinical Engineer.
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| Expert in Pharmaceutical and Device GMPs and sterilization.
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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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| 25 yrs experience w/medical equipment,Registered and Certified engineer. Director, Biomedical Engineering Dpt., Chairman technical standrads committees, Receipient FDA Commissioner Special Citation.
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| 30 years world-wide pharaceutical industry expertise in all aspects of GMP compliance and quality assurance. We know the FDA and we know what it takes to comply with GMP regulations
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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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| Bodycote Polymer is a materials technology consulting firm and laboratory specializing in failure analysis of plastic components and products, polymer analysis, and product development.
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| We can provide a world-class level of scientific advice and technical support to your claim, backed by
significant experience in advising on claims for damages involving rejected consignments of fishery products....
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| testifying expert on medication and vaccine adverse effects, FDA.
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| 30 years experience - all aspects of medical devices; Broad range of products; 31 patents; PI, PL & IP; Landmark cases; Plaintiff/defense; Seasoned, successful, affable; Impeccable references.
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| Qualified experts in toxic exposure cases since 1979. Asbestos-Industrial Hygiene-Environmental
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| Certified clinical engineer expertise: medical device safety, hospital accidents, and product liability.
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| Clinical Pharmacy, drug information services, pharmacology, pharmacokinetics, pharmacoepidemiology, pharmacoeconomics, adverse drug reactions/interactions, medication errors, under-dosing, narcotics.
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| Experts in the adhesive and coating industries with specialties in research, coating, manufacturing and quality control.
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| 27 years of experience in product design and manufacturing, premises design and maintenance, and accepted safety practices and accident prevention methods.
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| Expert in valuation of damages for business, information technology, software selection and implementation and web commerce, he has a quarter century of business and technology consulting experience.
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| Specializing in the review of product liability claims, identification, analysis and catagorizing hazards, misuses,misapplications of the product, the manufacturing process or the material involved.
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| Specializing in legal, educational and medical advice on toxicological issues.
Nationwide services with offices in Phoenix and New York/New Jersey.
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| Looking for a fda expert?
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Find Fda experts and consultants for Fda litigation support at www.findexperts.com. Available to be Fda expert witnesses and provide Fda forensic consulting in Fda litigation, in addition prepare Fda expert witness reports for use in deposition and/or in-court trial testimony.
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Categories To Find "Fda" Experts:
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BIOMEDICAL ENGINEERING |
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Biomedical engineers use their expertise in biology, medicine, physics, mathematics, engineering science and communication to make the world a healthier place. The biomedical engineer is ideally trained to work at the intersection of science, medicine and mathematics to solve biological and medical problems.
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CANCER - KIDNEY |
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Renal cell carcinoma, also known by the eponym Grawitz tumor, is the most common form of kidney cancer arising from the renal tubule. It is the most common type of kidney cancer in adults. Initial therapy is with surgery. It is notoriously resistant to radiation therapy and chemotherapy, although some cases respond to immunotherapy.
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CANCER - LUNG |
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Lung cancer is a cancer of the lungs characterised by the presence of malignant tumours. Most commonly it is bronchogenic carcinoma (about 90%). Lung cancer is one of the most lethal of cancers worldwide, causing up to 3 million deaths annually. Only one in ten patients diagnosed with this disease will survive the next five years. Although lung cancer was previously an illness that affected predominately men, the lung cancer rate for women has been increasing in the last few decades, which has been attributed to the rising ratio of female to male smokers.
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CONSUMER MARKETING |
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Find CONSUMER MARKETING experts and consultants for CONSUMER MARKETING litigation support. Available to be CONSUMER MARKETING expert witnesses and provide CONSUMER MARKETING forensic consulting in CONSUMER MARKETING litigation, in addition prepare CONSUMER MARKETING expert witness reports for use in deposition and/or in-court trial testimony.
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DERMATOLOGY |
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Dermatology (from Greek derma, "skin") is a branch of medicine dealing with the skin and its appendages (hair, nails, sweat glands etc). A medical doctor who specializes in dermatology is a dermatologist. The surgical practice of dermatology is dermasurgery.
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D.O.T. / REGULATORY COMPLIANCE |
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The United States Department of Transportation (DOT) is a Cabinet department of the United States government concerned with transport. It was established by an act of Congress on October 15, 1966 and began operation on April 1, 1967. It is administered by the United States Secretary of Transportation.
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While ADR is probably the most precise term to describe the concept, it is not widely used in the community since it may be perceived as jargon and because of the negative-associations with the term "drug". Alternative terms with equivalent meaning to ADR include: side-effect, adverse event, adverse effect, etc. Find Fda experts and witnesses in the DRUG INTERACTIONS & SIDE EFFECTS category." title="DRUG INTERACTIONS & SIDE EFFECTS SPECIALISTS -An adverse drug reaction (abbreviated ADR) is a term to describe the unwanted, negative consequences sometimes associated with the use of medications. ADR is a particular type of adverse effect. The term is preferred over the colloquial and imprecise "side-effect" as "side-effect" implies the potential for beneficial consequences.
While ADR is probably the most precise term to describe the concept, it is not widely used in the community since it may be perceived as jargon and because of the negative-associations with the term "drug". Alternative terms with equivalent meaning to ADR include: side-effect, adverse event, adverse effect, etc. Find Fda experts witnesses in the DRUG INTERACTIONS & SIDE EFFECTS category."> DRUG INTERACTIONS & SIDE EFFECTS |
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DRUG INTERACTIONS & SIDE EFFECTS SPECIALISTS -An adverse drug reaction (abbreviated ADR) is a term to describe the unwanted, negative consequences sometimes associated with the use of medications. ADR is a particular type of adverse effect. The term is preferred over the colloquial and imprecise "side-effect" as "side-effect" implies the potential for beneficial consequences.
While ADR is probably the most precise term to describe the concept, it is not widely used in the community since it may be perceived as jargon and because of the negative-associations with the term "drug". Alternative terms with equivalent meaning to ADR include: side-effect, adverse event, adverse effect, etc.
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FDA |
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The Food and Drug Administration (FDA) of the United States is the government agency responsible for regulating food (human and animal), dietary supplements, drugs (human and animal), cosmetics, medical devices (human and animal), biologics, and blood products in the United States.
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GMP - GOOD MANUFACTURING PRACTICES |
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Good Manufacturing Practice is a set of regulations, codes, and guidelines for the manufacture of drugs (known as medicinal products in Europe), medical devices, diagnostic products, foods products and Active Pharmaceutical Ingredients (APIs).
Since sampling products will statistically only ensure that the samples themselves (and perhaps the areas adjacent to where the samples were taken) are suitable for use, and end-point testing relies on sampling, GMP takes the holistic approach of regulating the production and laboratory testing environment itself. An extremely important part of GMPs is documenting every aspect of the process, activities, and of operations. If the documentation is not correct and in order, showing how the product was made and tested, that allows for traceability, and recall from the market in the event of future problems, then the product is considered contaminated (in the US considered adulterated).
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MEDICAL |
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Medical - Having to do with or anything pertaining to Medical treatment, Medical Malpractice, Medical review, Medical Litigation.
Find MEDICAL experts and consultants for MEDICAL litigation support. Available to be MEDICAL expert witnesses and provide MEDICAL forensic consulting in MEDICAL litigation, in addition prepare MEDICAL expert witness reports for use in deposition and/or in-court trial testimony.
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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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PHARMACEUTICAL LITIGATION |
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Thousands of people die from or are seriously injured by prescription and over-the-counter drugs each year. Patients trust these defective drugs will not harm them because they have been approved by the U.S. Food and Drug Administration or been prescribed by doctors or pharmacists they know and trust.
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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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PRODUCT SAFETY |
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The Consumer Product Safety Commission (CPSC) is an independent agency of the U.S. federal government created in 1972 through the Consumer Safety Act to protect against unreasonable risks of injuries associated with consumer products. As of 2005 its chairman is Hal Stratton, a Republican. The two other commissioners on the three-member board are (as of February 2006) Thomas Hill Moore (Democrat) and Nancy Nord (Republican).
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PTSD - POST TRAUMATIC STRESS DISORDER |
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Post-traumatic stress disorder (PTSD) is a term for certain psychological consequences of exposure to, or confrontation with, stressful experiences that the person experiences as highly traumatic. [1] These experiences can involve actual or threatened death, serious physical injury, or a threat to physical and/or psychological integrity. It is occasionally called post-traumatic stress reaction to emphasize that it is a routine result of traumatic experience rather than a manifestation of a pre-existing psychological weakness on the part of the patient.
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REGULATORY COMPLIANCE |
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Regulatory compliance refers to systems or departments at corporations and public agencies to ensure that personnel are aware of and take steps to comply with relevant laws and regulations.
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Fda Experts Witnesses - Fda Forensic Consultants.
Find Fda experts and consultants for Fda litigation support. Available to be Fda expert witnesses and provide Fda forensic consulting in Fda litigation, in addition prepare Fda expert witness reports for use in deposition and/or in-court trial testimony.
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