US Food Drug Administration

Source European Union (EU), US Food Drug Administration (FDA), and JECFA World Health Organization (WHO) regulations. ... [Pg.604]

HEALTH CANADA US,FOOD DRUG ADMINISTRATION HEALTH CARE WITHOUT HARM AMERICAN CHEMISTRY COUNCIL ... [Pg.56]

It is explained that the Food Contact Notification process of the US Food Drug Administration has been in place officially for three months This article asks, and then strives to answer, many questions about the system. [Pg.76]

EUROPEAN COMMISSION US,FOOD DRUG ADMINISTRATION GERMANY,FEDERAL MINISTRY FOR HEALTH EU EUROPEAN COMMUNITY EUROPEAN UNION ... [Pg.82]

EUROPEAN COUNCIL FOR PLASTICISERS INTERMEDIATES US,FOOD DRUG ADMINISTRATION US,ENVIRONMENTAL PROTECTION AGENCY... [Pg.98]

US,ENVIRONMENTAL PROTECTION AGENCY SOCIETY OF THE PLASTICS INDUSTRY US,FOOD DRUG ADMINISTRATION... [Pg.101]

While these external and internal factors already provided a difficult foundation, a routine investigation into the company by the US Food Drug Administration (FDA) identified areas of non-compliance with Good Manufacturing Practice (GMP) regulations. The resulting... [Pg.22]

US Food Drug Administration Center for Food Safety Applied Nutrition Foodbome Pathogenic Microorganisms and Natural Toxins Handbook - The Bad Bug Book . Online. Available HTTP (accessed 9 April 2003). [Pg.170]

Research at the US Food Drug Administration, stimulated me to suggest a specific term— pharmaco-informatics —to express the idea of a subdiscipline of pharmacology that focuses on the format and structure of the corpus of information that differentiates a medicine from a chemical. In the terms of the previous paragraph, it concerns the structure of the table of contents of the pharmaceutical user s manual . Transition to the infotensive age will... [Pg.240]

Reepmeyer JC, Cox DC (1987) FDA monograph guidelines to thalidomide synthesis. US Food Drug Administration, Washington, DC... [Pg.95]

Efavirenz (DMP 266) (1) is an effective non-nucleoside inhibitor of reverse transcriptase of the human immunodeficiency virus (HIV) recently registered by the US Food Drug Administration (FDA) for treatment of the acquired immunodeficiency syndrome (AIDS).1 2 3 Inhibition of HIV reverse transcriptase by nucleosides like azidothymidine (AZT) (2) is a proven therapy for delaying the progression to AIDS. However, the rapid viral mutation to resistant strains requires the development of new therapeutic agents. The recent development of both protease inhibitors and non-nucleoside reverse transcriptase inhibitors offers hope of effective treatment especially when coadministered. [Pg.71]

EnPol from Korea s IRe Chemicals are based on a group of aliphatic co-polyesters comprising adipic acid, succinic acid, 1,2-ethanediol or 1,4-butanediol. EnPol polymers meet the specifications of the US Food Drug Administration for food contact applications and the USP specifications for medical device applications. [Pg.25]

In 2004, Treofan GmbH developed a metallised version of its PLA biodegradable film that reduces permeability aromas, oxygen and water. The metallised Biophan PLA film is said to be suitable for packaging fatty foods such as butter and cheese, as well as for confectionery, where the mirror-like finish adds a decorative feature to the barrier properties. The metallised film meets both EU and US, Food Drug Administration food contact requirements. [Pg.69]

HEALTH NETWORK EASTMAN CHEMICAL EXXON BIOMEDICAL SCIENCES MASSACHUSETTS,INSTITUTE OF TECHNOLOGY HEALTH CARE WITHOUT HARM ADVAMED US,FOOD DRUG ADMINISTRATION VINYL INSTITUTE... [Pg.101]

Wells Plastics Ltd. of the UK, a compounder of additive masteibatches, has developed a technology that encapsulates silver ion anti-microbial systems within a soluble matrix. The silver ion formulations can help reduce infection in wound dressings, urinary catheters, and other medical applications. This article provides details. US,FOOD DRUG ADMINISTRATION WELLS PLASTICS LTD. [Pg.60]

US Food Drug Administration (2004) Pharmaceutical Current Good Manufacturing Practices (cGMPs) for the 2U Century - a Risk-Based Approach Final Report... [Pg.29]

Journal of Rubber Research 2, No.3, 3rd Quarter, 1999, p.131-9 ISSUES ASSOCIATED WITH USING FLUORESCENT MICROSPHERES TO EVALUATE THE BARRIER INTEGRITY OF NATURAL RUBBER LATEX FILMS Kaplan D A Lytle C D Routson L B Myers M R Alexandria,Thomas Jefferson High School for Science Technology US,Food Drug Administration... [Pg.84]

Gursel 1 Yagmurlu F Korksusuz F Hasirci V US,Food Drug Administration Ankara,Numune Hospital Ankara,Middle East Technical University... [Pg.81]

PUROLITE INTERNATIONAL DOW CHEMICAL CO. AP BIOTECH TOSOH BIOSEP LLC MITSUBISHI CHEMICAL AMERICA INC. AMERSHAM PHARMACIA BIOTECH AS BAYER AG SYBRON CHEMICALS INC. ROHM HAAS CO. TOSOHAAS TOSOH CORE US,FOOD DRUG ADMINISTRATION RESINTECH EUROPEAN COMMUNITY EUROPEAN UNION GERMANY JAPAN SCANDINAVIA SWEDEN UK USA WESTERN EUROPE... [Pg.89]

Journal of Applied Polymer Science 64, No.3, 18th April 1997, p.553-66 PERMEABILITY AND MATERIAL CHARACTERISTICS OF VULCANIZED LATEX FILM DURING AND FOLLOWING CYCLIC FATIGUE IN A SALINE ENVIRONMENT Dillon J G Schroeder L W US, Food Drug Administration... [Pg.51]

US, FOOD DRUG ADMINISTRATION US, NATIONAL BUREAU OF STANDARDS... [Pg.92]

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