During the period 1983 to 1987, VMI developed many " break through " IVR applications included both business and consumer related solutions: Stock Quotes for Dow Jones ; Flight Schedules for Pacific Southwest Airlines ; Drug Interactions for Physicians ’ Desk Reference ; Crew Scheduling for Trans World Airlines ; San Francisco Examiner, February 7, 1982 – Page 9.

* Pharmaceutical Press which published textbooks on a wide range of topics in pharmacy and pharmaceutical sciences, as well as the established Major Reference Works Martindale: The Complete Drug Reference, the British National Formulary and Stockley's Drugs Interactions

In addition to a drug reference phone line, where athletes can speak to an expert, USADA has partnered with UK Anti-Doping ( UKAD ) and the Canadian Centre for Ethics in Sport ( CCES ) to provide the Global Drug Reference Online ( GlobalDRO ) tool.

It features peer-reviewed original medical journal articles, CME ( Continuing Medical Education ), a customized version of the National Library of Medicine's MEDLINE database, daily medical news, major conference coverage, and drug information — including a drug database ( Medscape Drug Reference, or MDR ) and drug interaction checker.

A comparative analysis of Medscape Drug Reference versus Wikipedia concluded that drug monographs on Medscape Drug Reference were more comprehensive and Wikipedia articles had more errors of omission.

The HIV / AIDS Reference and Quality Assurance Laboratory ( HRL ), which is part of the institute plays an important role in making public policy recommendations to the Uganda National Drug Authority on the access and usage of new drugs and medical technologies.

* National Crime Justice Reference Service NCJ # 209084 and NCJ # 209085 Drug smuggling behavior

All the additives listed here are sanctioned for use by the Food and Drug Administration of the federal government.

Drug is added to either a protein or mineral supplement for a period of 7 or 14 days.

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.

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.

It is controlled by the WHO Collaborating Centre for Drug Statistics Methodology ( WHOCC ), and was first published in 1976.

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 regulations in are used to strictly limit, for instance, television receivers to 0. 5 milliroentgens per hour ( mR / h ) ( 0. 13 µC /( kg · h ) or 36 pA / kg ) at a distance of from any external surface ; since 2007, most CRTs have emissions that fall well below this limit.

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.

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.

* Drug Policy Alliance – 83 % for 2006

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 ).

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.

* Center for Drug Evaluation and Research ( CDER )

* U. S. FDA CDER Home Pagethe Center for Drug Evaluation and Research

This was the first evaluation of a lentiviral vector administered in U. S. Food and Drug Administration-approved human clinical trials for any disease.

This was the first evaluation of a lentiviral vector administered in U. S. Food and Drug Administration-approved human clinical trials for any disease.

Foods of this kind present a problem because the hidden gluten constitutes a hazard for people with celiac disease: In the United States, at least, gluten might not be listed on the labels of such foods because the U. S. Food and Drug Administration has classified gluten as GRAS ( generally recognized as safe ).

The HashKeeper database maintained by the American National Drug Intelligence Center, for instance, is more aptly described as a catalog of file fingerprints than of hash values.

Under his leadership, the company pioneered processes for sanitary food preparation, leading a successful lobbying effort in favor of the Pure Food and Drug Act in 1906.

*" The Nexus of Drug Trafficking and Hawala in Afghanistan ", Dr. Edwina A. Thompson, for the World Bank and the United Nations Office on Drugs and Crime ( UNODC )

Chinese immigrants were blamed for importing the opium-smoking habit to the U. S. The 1903 blue-ribbon citizens ' panel, the Committee on the Acquirement of the Drug Habit concluded, " If the Chinaman cannot get along without his dope we can get along without him.

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.

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.

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.

The Food and Drug Administration ( FDA or USFDA ) is an agency of the United States Department of Health and Human Services, one of the United States federal executive departments.

The FDA frequently works in conjunction with other federal agencies including the Department of Agriculture, Drug Enforcement Administration, Customs and Border Protection, and Consumer Product Safety Commission.

The U. S. Food and Drug Administration ( FDA ), with support from the TSE ( Transmissible spongiform encephalopathy ) Advisory Committee, has since 1997 been monitoring the potential risk of transmitting animal diseases, especially bovine spongiform encephalopathy ( BSE ), commonly known as Mad Cow disease.

For pharmaceutical grade gelatins strict regulations from the Food and Drug Administration ( FDA ), the European CPMP's regulation and European Pharmacopoeia must be met.

In consequence, the United States Department of Agriculture ( USDA ) has approved the use of low-level irradiation as an alternative treatment to pesticides for fruits and vegetables that are considered hosts to a number of insect pests, including fruit flies and seed weevils ; the U. S. Food and Drug Administration ( FDA ) has cleared among a number of other applications the treatment of hamburger patties to eliminate the residual risk of a contamination by a virulent E. coli.

However, the U. S. Food and Drug Administration ( FDA ) has not formally evaluated the effectiveness of these products.

The United States Food and Drug Administration ( FDA ) approved this off-label use of certain brands of regular combined oral contraceptive pills in 1997.

It is approved by the United States ' Food and Drug Administration ( FDA ) for the treatment of narcolepsy, shift work sleep disorder and excessive daytime sleepiness associated with obstructive sleep apnea.

In 2006, the U. S. Food and Drug Administration issued a caution about methadone, titled “ Methadone Use for Pain Control May Result in Death .” The FDA also revised the drug's package insert.

It was only until 1941 when estrogen therapy was finally approved by the Food and Drug Administration ( FDA ) for the treatment of menopausal symptoms.

Though not approved by the US Food and Drug Administration ( FDA ) for use on humans, obsidian is used by some surgeons for scalpel blades, as well-crafted obsidian blades have a cutting edge many times sharper than high-quality steel surgical scalpels, the cutting edge of the blade being only about 3 nanometers thick.

At the Federal level, consistent with Section 341 of the Federal Food, Drug, and Cosmetic Act, the Food and Drug Administration ( FDA ) has defined standards of identity for what are broadly termed macaroni and noodle products.

In March 2011 the U. S. Food and Drug Administration ( FDA ) notified healthcare professionals and the public that prescription proton pump inhibitor drugs may cause low serum magnesium levels ( hypomagnesemia ) if taken for prolonged periods of time-in most cases, longer than one year.

In response to a 1995 letter published in the New England Journal of Medicine, representatives of the U. S. Food and Drug Administration ( FDA ) stated the agency would " update the labeling insert for all marketed fluoroquinolones to include a warning about the possibility of tendon rupture.

From 1969 to 1992, the US Food and Drug Administration ( FDA ) received 157 reports of health problems related to quinine use, including 23 which had resulted in death.

The U. S. Food and Drug Administration ( FDA ) had documented design defects in medical devices that contributed to recalls from 1983 to 1989 that would have been prevented if Quality Systems had been in place.

In addition, in 2007 the U. S. Food and Drug Administration ( FDA ) approved an endotracheal breathing tube with a fine coat of silver for use in mechanical ventilation, after studies found it reduced the risk of ventilator-associated pneumonia.