Help


[permalink] [id link]
+
Page "Cathode ray tube" ¶ 18
from Wikipedia
Edit
Promote Demote Fragment Fix

Some Related Sentences

Food and Drug
All the additives listed here are sanctioned for use by the Food and Drug Administration of the federal government.
Acceptance of radiopasteurization is likely to be delayed, however, for two reasons: ( 1 ) the storage life of fresh chicken under refrigeration is becoming a minimal problem because of constantly improved sanitation and distributing practices, and ( 2 ) treatment by antibiotics, a measure already approved by the Federal Food and Drug Administration, serves to extend the storage life of chicken at a low cost of about 0.5 cents per pound.
For Mrs. Shaefer -- who had been given a clean bill of health by her own physician at the time she visited Lee -- and her friend were agents for the California Pure Food and Drug Inspection Bureau.
According to the Food And Drug Administration ( FDA ), `` Doctor '' Ghadiali, Dr. Albert Abrams and his clique, and Dr. Wilhelm Reich -- to name three notorious device quacks -- succeeded, respectively, in distributing 10,000, 5000, and 2000 fake health machines.
This task force aims to actively address antimicrobial resistance, and is coordinated by the US Centers for Disease Control and Prevention, the Food and Drug Administration ( FDA ), and the National Institutes of Health ( NIH ), as well as other US agencies.
In the United States the question of emergence of antibiotic-resistant bacterial strains due to use of antibiotics in livestock was raised by the United States Food and Drug Administration in 1977.
A review of both published and unpublished trials submitted to the U. S. Food and Drug Administration ( FDA ) found that the published trials had a 94 % success in treating depression while the unpublished literature had below 50 % success.
Amisulpride has not been approved for use by the Food and Drug Administration in the United States.
Since patents and regulation ( e. g., U. S. Food and Drug Administration regulation in the U. S .) are very important issues for biotech enterprises, bioengineers are often required to have knowledge related to these issues.
Nowadays, the agencies that are responsible for the biotechnology regulation are: US Department of Agriculture ( USDA ) that regulates plant pests and medical preparation from living organisms, Environmental Protection Agency ( EPA ) that regulates pesticides and herbicides, and the Food and Drug Administration ( FDA ) which ensures that the food and drug products are safe and effective
In the United States, the Food and Drug Administration has categorized benzodiazepines into either category D or X meaning potential for harm in the unborn has been demonstrated.
The Food and Drug Administration ( FDA ) is the principal healthcare regulatory authority in the United States, having jurisdiction over medical devices, drugs, biologics, and combination products.
On May 28, 2002, the United States Food and Drug Administration instituted a policy that excludes from donation anyone who spent at least six months in certain European countries, ( or three months in the United Kingdom ), from 1980 to 1996.
In 1986, the U. S. Food and Drug Administration banned the use of sulfites on fruits and vegetables intended to be eaten raw.
The center serves as the sole supplier of the active ingredients in two U. S. Food and Drug Administration-approved radiopharmaceuticals and produces Fluorine-18 used in PET imaging with its cyclotron.
The U. S. Food and Drug Administration calls this " sweet chocolate ", and requires a 15 % concentration of chocolate liquor.
Protein-bound paclitaxel ( e. g., Abraxane ) or nab-paclitaxel was approved by the U. S. Food and Drug Administration ( FDA ) in January 2005 for the treatment of refractory breast cancer.
When used as a medication in the U. S., coal tar preparations are considered an OTC ( over-the-counter drug ) pharmaceutical and are subject to regulation by the United States Food and Drug Administration.
The U. S. Food and Drug Administration regulates this practice by attempting to prevent the introduction of any part of a cow's brain or spinal cord into livestock feed.
Two federal agencies, the Drug Enforcement Administration and the Food and Drug Administration, determine which substances are added to or removed from the various schedules, though the statute passed by Congress created the initial listing, and Congress has sometimes scheduled other substances through legislation such as the Hillory J. Farias and Samantha Reid Date-Rape Prevention Act of 2000, which placed gamma hydroxybutyrate in Schedule I.
Digoxin was approved for heart failure in 1998 under current regulations by the Food and Drug Administration on the basis of prospective, randomized study and clinical trials.
Despite its relatively recent approval by the Food and Drug Administration and the guideline recommendations, digoxin use is decreasing in patients with heart failure, likely the result of several factors.
Availability-Currently there are 20 medications approved by the Food and Drug Administration for the use of treatment of epileptic seizures in the US: carbamazepine ( common US brand name Tegretol ), clorazepate ( Tranxene ), clonazepam ( Klonopin ), ethosuximide ( Zarontin ), felbamate ( Felbatol ), fosphenytoin ( Cerebyx ), gabapentin ( Neurontin ), lacosamide ( Vimpat ), lamotrigine ( Lamictal ), levetiracetam ( Keppra ), oxcarbazepine ( Trileptal ), phenobarbital ( Luminal ), phenytoin ( Dilantin ), pregabalin ( Lyrica ), primidone ( Mysoline ), tiagabine ( Gabitril ), topiramate ( Topamax ), valproate semisodium ( Depakote ), valproic acid ( Depakene ), and zonisamide ( Zonegran ).

Food and Administration
The Friedmans also argue for abolishing the Food and Drug Administration, tighter control of Fed money supply, and the repeal of laws favoring labor unions.
This overall budget covers core technical work, cooperation and partnerships, leading to Food and Agriculture Outcomes by 71 %; Core Functions by 11 %; the Country Office Network by 5 %; Capital and Security Expenditure by 2 %; Administration by 6 %; and Technical and Cooperation Program by 5 %.

Food and regulations
* Food labeling regulations
For pharmaceutical grade gelatins strict regulations from the Food and Drug Administration ( FDA ), the European CPMP's regulation and European Pharmacopoeia must be met.
The Radura logo, as required by U. S. Food and Drug Administration regulations to show a food has been treated with ionizing radiation.
* Food labeling regulations ( disambiguation )
In the United States, for example, U. S. Food and Drug Administration regulations prohibit marketing any magnet therapy product using medical claims, as such claims are unfounded.
Due to concerns over pests and pathogens, however, whole starfruits cannot yet be imported to the US from Malaysia under current Food and Drug Administration regulations.
The same year, the Doritos brand began complying with U. S. Food and Drug Administration labeling regulations, four years before the regulations became mandatory.
In the United States of America, tissue transplants are regulated by the U. S. Food and Drug Administration ( FDA ) which sets strict regulations on the safety of the transplants, primarily aimed at the prevention of the spread of communicable disease.
* Code of Federal Regulations, Title 21, Part 129 – U. S. Food and Drug Administration regulations on bottled water
Technically, the commercials complied with United States Food and Drug Administration regulations, and they were allowed to continue.
* Food labeling regulations
* Food labeling regulations
Food regulations for perishable goods prohibit it being sent abroad.
In the USA, because it is sold as a dietary supplement, sometimes combined with other ingredients, such as vitamins and herbal extracts, and not as a drug, the Food and Drug Administration ( FDA ) regulations that apply to medications are not applicable to melatonin.
While in most cases importation of prescription medications violates Food and Drug Administration ( FDA ) regulations and federal laws, enforcement is generally targeted at international drug suppliers, rather than consumers.
The U. S. Food and Drug Administration ( FDA ) regulations establish limits for contaminants in bottled water that must provide the same protection for public health.
In the framework of a multi-year collaboration IFOAM developed together with his UN partners: the Food and Agriculture Organization ( FAO ) and the United Nations Conference on Trade and Development ( UNCTAD ), a set of standard requirements that functions as an international reference to assess the quality and equivalency of organic standards and regulations.
In addition to its American stores, it maintains its own production facilities in China and these company-owned plants have implemented quality control measures to ensure that products from China are compliant with Food and Drug Administration standards and regulations.
In the United States, CES technology is classified by the Food and Drug Administration as Class III medical devices and must be dispensed by or on the order of a licensed healthcare practitioners, i. e. a physician, psychiatrist or nurse practitioner ; psychologists, physician assistants, and occupational therapists who have an appropriate electrotherapy license may prescribe CES, dependent upon state regulations.
Due to E. coli O157: H7 outbreaks from unpasteurized apple cider and other outbreaks from contaminated fruit juices, the U. S. Food and Drug Administration ( FDA ) proposed new regulations in 1998, and Canada followed suit in 2000.
The bulk of cider production and sale fell under the umbrella of proposed 1998 U. S. Food and Drug Administration regulations applying to all fresh fruit and vegetable juices.
One of the main acts and regulations that CFIA uses is the Food and Drugs Act, which was last updated in 1985.

0.379 seconds.