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Lindane - Stockholm Convention
Lindane - Stockholm Convention

... Scabies is a parasitic disease that ‘is a major public health problem in many resourcepoor regions. It causes substantial morbidity from secondary infections and post-infective complications such as acute post-streptococcal glomerulonephritis.” Scabies is strongly associated with poverty and overcro ...
Evaluation of Quality Control Parameters of Two Brands of
Evaluation of Quality Control Parameters of Two Brands of

SHPA Medicines Information Procedure Manual
SHPA Medicines Information Procedure Manual

... and maintain a medicines information (MI) service. In this manual, medicines information (MI) refers to information or advice provided in response to a request from a health professional, organisation, or consumer and may relate to a specific patient, or consists of general information promoting the ...
O A
O A

... The best results were obtained by using 16 nm as Δλ a scaling factor = 100 in order to diminish the error in reading the signal. Figures (3-5) show that it can be determined at 256.4 nm, 269.8 and 226.6 nm for D2, D3 and D4 respectively which correspond to the zero crossing points of its degradate. ...
- Fred Help Centre
- Fred Help Centre

... • Safer – visibility over a patient’s combined prescribed and dispensed medications history gives you the ability to monitor regime compliance and limit adverse drug interactions. • Discharge information – See hospital discharge medications to ensure continuity of care. • Efficient – giving you the ...
DEVELOPMENT AND VALIDATION OF A RP-HPLC METHOD FOR SIMULTANEOUS
DEVELOPMENT AND VALIDATION OF A RP-HPLC METHOD FOR SIMULTANEOUS

... Recovery studies: For both drugs recovery studies were carried out by applying the method to drug sample to which known amount of Pantoprazole and Cinitapride corresponding to 80, 100 and 120 % of label claim had been added (Standard addition method). At each level three determinations were carried ...
OVERVIEW OF CHIRALITY AND CHIRAL DRUGS
OVERVIEW OF CHIRALITY AND CHIRAL DRUGS

... seeds and is tasteless, while the d -form is sweet. Thalidomide is another classical example. It was first synthesized as a racemate in 1953 and was widely prescribed for morning sickness from 1957 to 1962 in the European countries and Canada. This led to an estimated over 10,000 babies born with de ...
IOSR Journal of Pharmacy and Biological Sciences (IOSRJPBS)
IOSR Journal of Pharmacy and Biological Sciences (IOSRJPBS)

... For analysis of commercial formulations of tablets, 10 tablets were weighed, powdered and accurately weighed the equivalent to 25 mg of atenolol and 12.5mg of chlorthalidone, which was transferred into 100 ml volumetric flask and in methanol and make up to 100ml with methanol, filtered and further d ...
How appropriate is antibacterial use in the community?
How appropriate is antibacterial use in the community?

Benzodiazepine usage in the North Eastern Health Board
Benzodiazepine usage in the North Eastern Health Board

... the benzodiazepine-related drugs zolpidem and zopiclone. The total average number of Defined Daily Doses (DDDs) per prescription items for all included drugs was for the period for 22 days supply. All the hypnotics had average number of DDDs per prescription higher than the recommend, for 14 days su ...
ANALYTICAL METHOD DEVELOPMENT AND METHOD VALIDATION FOR THE ESTIMATION
ANALYTICAL METHOD DEVELOPMENT AND METHOD VALIDATION FOR THE ESTIMATION

... Several HPLC methods have been reported for determining pioglitazone hydrochloride[1] in tablets. The quantitative determination of pioglitazone in human serum by direct-injection HPLC mass spectrometry and its application to a bioequivalence study has also been reported. Yamashita determined piogli ...
Brimonidine Tartrate 0.2% w/v Eye Drops
Brimonidine Tartrate 0.2% w/v Eye Drops

united states district court
united states district court

Scope of Practice for Naturopathic Physicians – Standards, Limits
Scope of Practice for Naturopathic Physicians – Standards, Limits

... consider carefully the commitment of time, resources and personal involvement of the registrant that meeting such standards will require before making application for such approval. Such authorization will rarely be granted. Factors such as extreme geographic isolation and lack of alternative source ...
ASIAN JOURNAL OF PHARMACEUTICAL SCIENCES
ASIAN JOURNAL OF PHARMACEUTICAL SCIENCES

... excipients or products. This allows each company to determine which solvents it uses in production and develop testing procedures that address their specific needs. It is the responsibility of the drug manufacturer to qualify the purity of all the components used in the manufacturing of the drug pro ...
Biowaiver monographs for immediate release solid oral dosage forms
Biowaiver monographs for immediate release solid oral dosage forms

... and one liquid acetaminophen product for their comparative BA, reporting a BA relative to the liquid dosage form of 82%, 87%, and 92%, respectively. However, based on urinary excretion data, these differences were not statistically significant and only the amount excreted from 0 to 4 h varied with t ...
Testosterone undecanoate
Testosterone undecanoate

Ferrario A, Kanavos P, Managed entry agreements for pharmaceuticals: the European experience. EMiNet, Brussels, Belgium
Ferrario A, Kanavos P, Managed entry agreements for pharmaceuticals: the European experience. EMiNet, Brussels, Belgium

... reimbursement lists need to demonstrate that their drugs can provide additional benefit in relation to current therapies and value-for-money in order to obtain coverage. Data and the overall evidence base available at registration are often insufficient to accurately estimate the clinical and cost-e ...
History of TYLENOL - Nancy West Communications
History of TYLENOL - Nancy West Communications

... had been investigating naphthalene for its beneficial effect in the treatment of this problem. When their drug supply ran out, they ordered more from a local pharmacy. An inexperienced pharmacist mistakenly filled the prescription with acetanilide. (Although discovered in 1852 by the French chemist ...
House Holds Hearing on FDA`s Authority over Compounding
House Holds Hearing on FDA`s Authority over Compounding

... Despite these observations, FDA maintains that it has authority to regulate compounding. The Food, Drug, and Cosmetic Act (FDCA) forbids introducing any “new drug” into interstate commerce without FDA approval6 and under this provision, FDA has for many years maintained that pharmacy-compounded drug ...
abstracts
abstracts

UTILITY OF BROMOSUCCINIMIDE AS AN ENVIRONMENTAL-FRIENDLY REAGENT FOR SENSITIVE Innovare
UTILITY OF BROMOSUCCINIMIDE AS AN ENVIRONMENTAL-FRIENDLY REAGENT FOR SENSITIVE Innovare

... Sp. gr. 1.18, 37%) to 100 mL with bidistilled water and standardized as recommended previously[37] prior to use. Methyl orange (50 μg mL-1): A 500 μg mL-1 dye solution was first prepared by dissolving accurately weighed 58.8 mg of dye (Sigma-aldrish, 85 % dye content) in water and diluting to 100 mL ...
Pharmaceutical Blister Packaging, Part I
Pharmaceutical Blister Packaging, Part I

Association between KEGG Biological Pathways and Adverse Drug
Association between KEGG Biological Pathways and Adverse Drug

... KEGG (Kyoto Encyclopedia of Genes and Genomes) is a collection of databases dealing with genomes, biological pathways, diseases, drugs, and chemical substances. KEGG is utilized for bioinformatics research and education, including data analysis in genomics, metagenomics, metabolomics and other omics ...
here.
here.

... high quality care. The QOF has had considerable influence on the way GPs work, including their prescribing. For example, it includes targets for managing particular conditions, such as hypertension, which have an effect on prescribing. 4. Prescribing is also influenced by clinical guidelines, which ...
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Pharmaceutical marketing

Pharmaceutical marketing, sometimes called medico-marketing or pharma marketing in some countries, is the business of advertising or otherwise promoting the sale of pharmaceuticals or drugs.Many countries have measures in place to limit advertising by pharmaceutical companies.Pharmaceutical company spending on marketing far exceeds that of its research budget. In Canada, $1.7 billion was spent in 2004 to market drugs to physicians; in the United States, $21 billion was spent in 2002. In 2005, money spent on pharmaceutical marketing in the United States was estimated at $29.9 billion with one estimate as high as $57 billion. When the U.S. numbers are broken down, 56% was free samples, 25% was pharmaceutical sales representative ""detailing"" (promoting drugs directly to) physicians, 12.5% was direct to user advertising, 4% on detailing to hospitals, and 2% on journal ads. There is some evidence that marketing practices can negatively affect both patients and the health care profession.
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