Drug Administration

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Government Spotlight: Food and Drug Administration

43 days ago

Ohio Tomatoes Cleared by U.S. Food and Drug Administration

Source: news.yahoo.com --- 45 days ago
The U.S. Food and Drug Administration (FDA) recently added Ohio to a list of states that are not associated with the latest food safety alert for certain types of raw red tomatoes and products containing raw red tomatoes, due to an outbreak of salmonellosis. ...

Pharmavite Prepared for U.S. Food and Drug Administration's Dietary Supplement Good Manufacturing Practice Gui

Source: www.moreover.com --- 43 days ago
NORTHRIDGE, Calif. - (Business Wire) More than 150 million Americans take dietary supplements annually, helping create a $24.1 billion industry. ...

Inhaled anesthesia: the original closed-loop Drug Administration paradigm.

Source: www.ncbi.nlm.nih.gov --- 34 days ago
Related Articles Inhaled anesthesia: the original closed-loop Drug Administration paradigm. Clin Pharmacol Ther. 2008 Jul;84(1):15-8 Authors: Gupta DK, Eger EI We administer anesthetics to obtain therapeutic effects and minimize untoward side effects. Anesthetists can precisely control inhaled anesthetic concentrations by controlling end-tidal volatile anesthetic concentrations. This degree of control eliminates the need for closed-loop inhaled anesthetic systems. The low solubility of modern inhaled anesthetics adds to the stability and control of the anesthetic state; the effective inhaled concentration varies little during maintenance of anesthesia unless altered by the anesthetist. A less precise closed-loop system applies a processed electroencephalogram (EEG) to assess depth of anesthesia and enable accurate delivery of volatile and intravenous anesthetics to maintain a stable state of anesthesia. PMID: 18563068 [PubMed - in process] ...

Federal Register: Guidance for Industry and Food and Drug Administration Staff; Surveillance and Detention Without Physical Examination of Condoms; Availability.

Source: www.fda.gov --- 13 days ago
This guidance document provides information to FDA staff and industry about FDA's strategy for addressing further imports of condoms from manufacturers/shippers whose condoms have failed to meet FDA's minimum acceptable quality criteria. ...

Federal Register: Food and Drug Administration Critical Path Workshop on Clinical Trials for Local Treatment of Breast Cancer by Thermal Ablation.

Source: www.fda.gov --- 3 days ago
The FDA is is announcing a public workshop to discuss the issues associated with the development and implementation of feasibility trials for local treatment of breast cancer by thermal ablation. ...

Federal Register: Guidance for Industry and Food and Drug Administration Staff; Surveillance and Detention Without Physical Examination of Surgeons' and/or Patient Examination Gloves; Availability.

Source: www.fda.gov --- 13 days ago
This guidance document provides information to FDA staff and industry about FDA's strategy for addressing further imports of surgeons' and patient examination gloves (medical gloves) from manufacturers/shippers whose medical gloves have failed to meet... ...

Allergan Receives U.S. Food and Drug Administration Approval for TRIVARIS(TM) (triamcinolone acetonide injectable suspension) 80 mg/mL

Source: www.businesswire.com --- 38 days ago
IRVINE, Calif.--(BUSINESS WIRE)--Allergan, Inc. (NYSE: AGN) today announced that the U.S. Food and Drug Administration (FDA) has approved TRIVARIS ...

Vermillion Files 510(k) Application With U.S. Food & Drug Administration For OVA1 Ovarian Tumor Triage Test

Source: www.medicalnewstoday.com --- 28 days ago
Vermillion, Inc. (Nasdaq: VRML), a molecular diagnostics company, announced that it has submitted a 510(k) pre-market notification application to the U.S. Food & Drug Administration (FDA) requesting regulatory clearance of its Ovarian Tumor Triage Test known as OVA1(TM). ...

Pharmavite Prepared for U.S. Food and Drug Administration's Dietary Supplement Good Manufacturing Practice Guidelines

Source: www.moreover.com --- 43 days ago
Earthtimes.org Jun 12 2008 1:43PM GMT ...

Bush Administration Settles Nationwide Class Action in Medicare Prescription Drug Case

Source: www.moreover.com --- 35 days ago
Yahoo! Canada Jun 19 2008 5:50PM GMT ...

(Crain€™s) € A consumer watchdog group says Kraft Foods Inc. is among companies making €bogus claims€ about the health benefits of their products, and it wants the Food and Drug Administration to step in. The Cent

Source: www.moreover.com --- 23 days ago
Crains ChicagoBusiness Jul 1 2008 9:05PM GMT ...

Drug Enforcement Administration To Propose Rule To Allow E-Prescribing Of Controlled Substances

Source: www.medicalnewstoday.com --- 32 days ago
The Drug Enforcement Administration as early as next week plans to announce a proposed rule that would allow electronic prescribing of medications classified as controlled substances, according to an individual familiar with the situation, the Wall Street Journal reports. ...

UNLISTED biotech Hunter Immunology has become the latest Australian company to near late stage clinical trials, after the company submitted an Investigational New Drug application with the US Food and Drug Administration to begin a Phase 3 clinical t

Source: www.moreover.com --- 16 days ago
BioTechnologyNews.net Jul 8 2008 6:58PM GMT ...

Food and Drug Administration reports more cases of salmonella illnesses

Source: www.moreover.com --- 19 days ago
Canada East Jul 5 2008 11:02PM GMT ...

Arthritis Foundation Comment On Food And Drug Administration Ongoing Safety Review Of Tumor Necrosis Factor (TNF) Blockers

Source: www.medicalnewstoday.com --- 44 days ago
The Food and Drug Administration (FDA) issued an early communication on June 4, 2008 regarding an ongoing safety review of Tumor Necrosis Factor (TNF) Blockers (marketed as Remicade, Enbrel, Humira, and Cimzia) and the possible association between the use of these medicines and the development of lymphoma and other cancers in children and young adults. ...

Food and Drug Administration/Tomato-linked Salmonella Outbreak :

Source: www.ktvl.com --- 45 days ago
www.fda.gov/oc/opacom/hottopics/tomatoes.html#retailers. ...

NORML.ORG US Drug Enforcement Administration Celebrates 35 Years Of Failure

Source: www.norml.org --- 18 days ago
(Thu, 03 Jul 2008) ...

Bush Administration Asks for Authority to Approve Generic Biologics; U.K. to Require Earlier Release of Adverse Trial Data; FDA Plans More Communication on Drug Risks; FDA Sets Out Rules for Distribution of Papers on Unapproved Uses; Grassley Asks GAO to Probe FDA Approvals; Supreme Court Splits on Rezulin Question; Medical Device Amendments Shield Manufac

Source: www.liebertonline.com --- 12 days ago
Biotechnology Law Report Jun 2008, Vol. 27, No. 3: 206-215. ...

Visionsense Announces Food and Drug Administration (FDA) 510(k) Clearance for Neurosurgery

Source: www.primenewswire.com --- 23 days ago
ORANGEBURG, N.Y., July 2, 2008 (PRIME NEWSWIRE) -- Visionsense Corp. announces FDA 510(k) Clearance of the new VSII -- Visionsense Stereoscopic Vision System for use in MIS Neurosurgery. ...

Oral Testimony Of CFTC Acting Chairman Walter Lukken, House Appropriations Subcommittee On Agriculture Rural Development, Food And Drug Administration, And Related Agencies

Source: www.mondovisione.com --- 13 days ago
Click here to download the oral testimony of CFTC Acting Chairman Walter Lukken, House Appropriations Subcommittee on Agriculture Rural Development, Food and Drug Administration, and Related Agencies. ...

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