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Syllabus
Syllabus

... ix. Patents Act 1970 and Rules 1972 4. International documentation: New drug application. Relevant information for marketing the Pharmaceutical products in other countries, IPR studies, Procedure of filling patent (National & International). ...
Pharmaceutical Price Policies and Practices in China
Pharmaceutical Price Policies and Practices in China

... Health Economics Institute, 2006 #32}. Due to information asymmetry, patients have no power to control the quality and amount of medical services, and have to rely on physicians to make decisions on their behalf. So, hospitals and physicians can boost drug sales. In 2005, hospitals’ margins were ove ...
The Beginnings: Laboratory and Animal Studies: From Test Tube to
The Beginnings: Laboratory and Animal Studies: From Test Tube to

... of its breakdown products (metabolites), and how quickly the drug and its metabolites are excreted from the body. Sometimes, such tests find a metabolite that is more effective than the drug originally picked for development. Of particular concern is how much of the drug is absorbed into the blood. ...
Drug Wastage Corporate Medical Policy Policy
Drug Wastage Corporate Medical Policy Policy

... 1. Drug wastage is documented in the patient’s medical record with date, time, amount administered, amount wasted and reason for wastage. Upon review, any discrepancy between amount administered to the patient and amount billed will be denied as nonrendered unless the wastage is clearly and acceptab ...
to our FREE PDF, “Drugs
to our FREE PDF, “Drugs

... Clear Recovery Center is an outpatient recovery facility located in Redondo Beach, CA. Through our staff ’s extensive experience, we have accumulated a lot of useful information about what drugs are, what they look like and what they do. We decided to create a “Drugs & Youth” informational booklet ...
The results of study on Unoprostone (development code UF-021) for... the 30th Annual Meeting of the Japan Society of Drug...
The results of study on Unoprostone (development code UF-021) for... the 30th Annual Meeting of the Japan Society of Drug...

... normal tension glaucoma. Since its release in 1994, it has been approved in 45 countries. In 2009 the concentration of preservative contained in Rescula® Eye Drops 0.12% was reduced by a change in the formulation, and in 2010 storage at room temperature instead of in a cold place became possible. Re ...
Medicine is a constantly changing field that demands breakthroughs
Medicine is a constantly changing field that demands breakthroughs

Collection of Real World Data in the Context of Rare
Collection of Real World Data in the Context of Rare

... Expanded access is usually given: + on a case-by-case basis for an individual patient; + for intermediate-size groups of patients with similar treatment needs who otherwise do not qualify to participate in a clinical trial; + for large groups of patients who do not have other treatment options avail ...
Mannitol Glass vial Product Sheet (PDF - 10 Ko)
Mannitol Glass vial Product Sheet (PDF - 10 Ko)

Continuing evolution of the drug discovery process in
Continuing evolution of the drug discovery process in

Drug Discovery 3
Drug Discovery 3

... compound from the other inactive substances • Lastly, a structural determination will need to be made ...
NEW SPECTROPHOTOMETRIC ESTIMATION OF PRULIFLOXACIN USING 2,4- DINITROPHENYL HYDRAZINE REAGENT Research Article
NEW SPECTROPHOTOMETRIC ESTIMATION OF PRULIFLOXACIN USING 2,4- DINITROPHENYL HYDRAZINE REAGENT Research Article

... addition- elimination reaction to give coloured chromogen. Beer’s law is obeyed in the range of 1-7 µg/ml for Prulifloxacin. Optimization of parameter The optimum concentration and volume were selected on the basis of their ability to give maximum absorbance. By varying one and keeping other experim ...
Diovan (Chronic Heart Failure) - Forecast and Market Analysis to... Brochure
Diovan (Chronic Heart Failure) - Forecast and Market Analysis to... Brochure

... continue to demonstrate the drug’s efficacy in patients with heart failure with preserved ejection fraction (HF -PEF), and it gains approval for use in this population, it will be the first drug to show efficacy in this largely underserved patient population. In addition, increased use of MRAs over ...
Herbal Compositions for Appetite Suppression and Weight
Herbal Compositions for Appetite Suppression and Weight

... *Corresponding author: Mesfin Yimam, Unigen, Inc. 3005 1st Ave, Seattle WA 98121, Tel: 206-629-3040; Email: [email protected] ...
Remeron (mirtazapine) - The Main Line Center for the Family
Remeron (mirtazapine) - The Main Line Center for the Family

BIOM 255: Molecular basis of drug action and disease therapy
BIOM 255: Molecular basis of drug action and disease therapy

... Accumulated evidence suggests that the placebo effect is a genuine psychobiological event attributable to the overall therapeutic context. This psychosocial context can consist of individual patient and clinician factors, and the interaction between the patient, clinician, and treatment environment ...
Full text
Full text

... In September 2010, cases of systemic allergy in users of a soap bar containing hydrolyzed wheat powder were reported from medical institutions. The cases of systemic allergy were published in October 2010 to raise an alert.1) The reported food allergy with systemic symptoms, which may be due to tran ...
Chelation
Chelation

... recommended by mainstream authorities, risk losing their licences and all that it entails. The benefits of these treatments can often be demonstrated by clinical observation and further verified by clinical tests. Pharmaceutical firms are not interested in this particular approach as there is no mon ...
Attachment A Comments in Response to the Food and Drug Administration
Attachment A Comments in Response to the Food and Drug Administration

... Investigational Drugs for Treatment Use (71 Fed. Reg. 75147) and the second NPRM addressed Charging for Investigational Drugs (71 Fed. Reg. 75168). The issues highlighted below correspond with those noted in the NPRMs. Improving Patient Information and Consent Issue : FDA regulatory requirements sho ...
What is pharmaceutics? - University of Toronto
What is pharmaceutics? - University of Toronto

... • Deals with many aspects of interactions both inside and outside the body • It’s not trivial to design and implement a dosage form that is both safe and effective for the drug’s intended use! ...
The Ethics of Pharmaceutical Industry Influence in Medicine (English)
The Ethics of Pharmaceutical Industry Influence in Medicine (English)

... including the prestigious Rappeport Fellowship, awarded to a few residents throughout the United States who have a strong background in psychiatry and the law. Robindra Paul, M.D., D.P.H., M.B.A. is a psychiatrist in private practice in San Diego, California. He is board certified in psychiatry and ...
False-positive DOA testing results due to prescription
False-positive DOA testing results due to prescription

... pseudoephedrine, ephedrine, or other sympathomimetic amines interfere with screening tests for amphetamines but do not cause positive test results in the gas chromatography/ mass spectrometric, or GC/MS, confirmation, thus pose no serious challenge in drugs-of-abuse (DOA) testing. In contrast, sever ...
department/course
department/course

... want to ask a question in front of the entire class, talk to your instructor or other students when there is free time within the classroom. (There will be frequent opportunities at the end of class sessions to get clarification) Asking classmates questions while other classroom information is takin ...
Direct5
Direct5

... • Marketers are tapping into blogs as a medium for reaching carefully targeted consumers. • Firms should monitor blogs for what is being said. ...
investigator brochure - University Hospitals of Leicester
investigator brochure - University Hospitals of Leicester

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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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