FDA Prehistory - Research

FDA Prehistory - Research

Chapter 14 The Food and Drug Administration FDA Prehistory 1862, President Lincoln appointed first director of Department of Agriculture 1883 Request for petition to pass laws prohibiting adulteration & misbranding of foods and drugs. For serious drinking, the drugstore was the place to go. Lydia E. Pinkham's Vegetable Compound, a popular nostrum for women, was depending on the formula, 15 to 20 percent alcohol (VU).

Advertising Cards A common method for medicine-makers to hawk their products was to provide druggists with postcard-sized advertisements with a picture on one side and a description of the glories of the product on the other. Ayer's Sarsaparilla Dr. Morse's Indian Root Pills Hires' Root Beer Lydia E. Pinkham's Vegetable Compound (First Card) Lydia E. Pinkham's Vegetable Compound (Second Card)

Pond's Extract Rumford Yeast Powder Wells, Richardson, & Co.'s Lactated Food http://www.mc.vanderbilt.edu/biolib/hc/nostrums/cards.html The Jungle, Upton Sinclair, 1906 with the hot weather there descended upon Packingtown a veritable Egyptian plague of flies; there could be no describing this--the houses would be black with them. There was no escaping; you might provide all your doors and windows

with screens, but their buzzing outside would be like the swarming of bees, and whenever you opened the door they would rush in as if a storm of wind were driving them. (Chapter 10) FDA History 1906: FDA formed, banned interstate commerce in adulterated misbranded food, drink, and drugs 1938 107 deaths of (primarily) children due to ingestion of Elixir of Sulfanilamide, a toxic combination of diethylene glycol and sulfa.

=>1938 Federal Food, Drug and Cosmetic Act FDA Act 1938 requiring that new drugs be shown to be safe before marketing. extending FDAs control to cosmetics and therapeutic devices. authorizing factory inspections and standards of identity for food staples. eliminating a requirement to prove intent to defraud in drug misbranding cases. adding court injunctions to the previous penalties of

seizures and prosecutions Drug Testing Guidelines: 1. Chemical Composition 2. Acute toxicity studies in two species 3. Chronic toxicity studies with different doses in different species 4. Observation of animals 5. Pathological examination of animals 6. Studies on the absorption and elimination of the chemical 7. Study of interactions

8. Knowledge of idiosyncrasies and untoward reactions http://www.mtn.org/quack/ Get Rid of the Spectacle Nuisance Regain Your Eye Freedom SIMPLY-SATISFACTORILY-SAFELY The Natural Eyesight System Tells You How No Doctoring-No Drugs-No Danger

Nothing to Wear and Nothing to Fear The Crystaldyne Pain Reliever, 1996 Similar to The Stimulator The Stimulator is essentially an electric gas barbecue grill igniter outfitted with finger grips. When pressed against the skin, the devices sparks and causes a small electric shock. Makers of the device claim it can relieve headaches, back pain, arthritis, stress, menstrual cramps, earaches, sinus, nosebleeds, flu and other ailments. Because of its medical claims, the Stimulator is considered a medical device. The manufacturers, however, have not complied with any FDA regulations that govern the marketing of medical

devices. The companies have submitted no information to FDA showing that the device is either safe or effective... FDA History Continued 1962 sale/use of thalidomide banned in U.S. based upon thousands of birth defects, primarily in Europe & South America amendment for efficacy & safety 1969 hearings re injuries (10,000) & deaths (731) in a 10 year period [heart valves, pacemakers, IUDs, (Nader)]

FDA History Continued => 1976 Medical Device Amendments [new=> review, old=>grandfathered, new equivalent=>grandfathered] =>1978 Good Manufacturing Practices =>1984 Medical Device Reporting =>1988 Device Recall/Rebuild =>1990 Safe Medical Devices FDA History Continued =>1992 Medical Device Amendments [tracking, surveillance, reporting, refund, ..]

=>1997 Modernization Act: public health is a responsibility shared by the entire health care community. The law directs the agency to carry out its mission in consultations and cooperation with all FDA stakeholders, including consumer and patient groups, the regulated industry, health care professionals, and FDAs regulatory counterparts abroad Labeling FDA (also) regulates the labeling of products under its jurisdiction. This information, which

must be rigorously truthful, well documented, and not misleading, plays a major role in protecting consumers and the public health. The FDAregulated food label is helping shoppers eat a healthy diet; the labeling of drugs and medical devices gives prescribers and patients reliable guidance about the safety and effectiveness of health care products. Recent TV Ad (October 2001)

(several photos of couples, ) 3 bottles of male virility compounds! Free three month supply, 3 bottles! Simply pay $8.50 shipping and handling charges for each bottle! No health claims are made for these pills in accordance with FDA regulations. 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 it's 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." FDA Definition

Is My Device a Medical Device? http://www.fda.gov/cdrh/devadvice/11.html#start http://www.fda.gov/cdrh/devadvice/313.html http://www.fda.gov/cdrh/devadvice/3132.html#class_1

http://www.fda.gov/cdrh/devadvice/3132.html#class2 http://www.fda.gov/cdrh/devadvice/3132.html#class2 http://www.fda.gov/cdrh/devadvice/3131.html#proceed Special Terms

510k Premarket notification IDE investigational device exemption PMAA premarket approval application GLP good laboratory practices GMP good manufacturing practices Design Control IRB Institutional review board Class 1

Not life sustaining No risk No standards 510k (some) => registration => listing => GMP (some) => Record keeping Tongue depressors, stethoscopes*, screwdrivers, Class 2

Not life sustaining, but must meet control/performance standards 510k => IDE => PMAA => Registration => Record keeping Sphygmanometer, powered wheelchairs, drapes, infusion pumps Class 3 Life sustaining 510k => IDE => [data!!!] => PMAA => Registration => Record Keeping Data & techniques must include failure

mode analysis, animal test, toxicology studies, human trials (IRB), PDP (product development protocol.) FDA approval? One or more years Now you will be monitored Registration (All US (foreign optional))+ (manufacturer or preparer or processor or propagator of device) must register yearly with FDA &

get a device registration #. (30 days change) Listing All manufacturers must list w FDA all devices they market (q 6 mo.) All manufacturers must supply FDA with all labeling & advance copy of new labeling. Registration + Listing = traceability & recallability

FDA may force recall, fines, reparations, repair, FDA may inspect devices, records, labeling, documentation, licenses, laboratories, premises, etc at virtually any time. FDA requires reporting of adverse events (MAUDE system.) Software If part of a device, generally must meet same minimum standards as the device. If standalone (say drug calculator) same

general levels: I = no risk, II = some, esp. if in radiation therapy machines, III = life sustaining 8-20% of all deaths are software related. Drugs FDA has even more say here. All drugs must be tested on at least 2 properly chosen animal models (thalidomide). (Generally do test tube toxicity test first, then animals.) Testing on humans must go through three or more stages under IRB control. Testing must stop if

there is any untoward event. Powers: fine, recall, inspect, etc. Animals? Chimpanzees, cats, dogs, mice/rats**, primates, rabbits, pigs, sheep, ferrets, woodchuck, armadillo, guinea pigs, lobsters, chinchillas, electric eels, opossums, angler fish, axolotl, slugs, pigeons, shark, zebra fish, tropical fish, trout, goldfish, C elegan, fruit fly, etc.

Drug testing in Humans Under IRB approval: (Informed consent) Phase 1: small cohort, 20-80 people, look for major problems, safety, tolerance, dose limiting toxicities, mode of entry, dose range Phase 2: 100 - 300, look for dosing concerns, look for minor problems, efficacy, safety Phase 3: 1000-3000 develop and prove statistics on efficacy, safety, tolerance, possible other uses. FDA Approval? Screen 5000 compounds => 5 trials => 1

drug. Blind/Double blind studies High cost of development ($360M), giving rise to mathematical modeling & simulation Penalties! $100M fine Abbott Labs Q/A. http://www.apexbioscience.com/products.htm For more detailed information on PHP, click here) Indications:

Nitric Oxide-induced shock Other proprietary applications Status: Established patent position

Proved NO scavenger concept in sheep, dog, pig, and mouse models Completed Phase 1 safety study and initial Phase 1/2 patient trial for NO-induced shock Completed continuous infusion and dose escalation (Phase 2) clinical trial Randomized, controlled Phase 3 trial to commence in 2001

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