‚ 2008; Grabowski et al.‚ 2011) have discussed the advantages and disadvantages of manufacturing authorized and unauthorized generic drugs. This issue is controversial because it involves the interests of a wide range of stakeholders‚ such as pharmaceutical companies‚ governments and the general public. Although there are numerous factors involved‚ opinions on the situation can be divided into four general areas‚ political‚ economic‚ health-related and technological. Those who support manufacture
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qd * Zoloft 100 mg qd * Synthroid 0.25 mg qd * Detrol XL 4 mg qd * Norpace 150 mg bid * Inderal 80 mg bid * Bumex 2 mg qd * Aldactone 100 mg qd * Avapro 300 mg qd * Prinivil 40 mg qd * Glucophage 850 mg bid DESYREL (1) 300 mg bid The active pharmaceutical ingredient in it is trazadone‚ an oral drug available as a regular/extended release tablet to be taken twice daily. STRUCTURE MECHANISM OF ACTION It is a selective serotonin receptor inhibitor that inhibits reuptake of serotonin and causes subsensitivity
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RESUME RAVAL KAVIT HARSIDDHARAY Department of Pharmaceutical Engineering‚IIT-BHU‚Varanasi. Mob no: 08081930031 Email id: raval.kavit.phe11@itbhu.ac.in Objective: To be potential resource to the organization where I can utilize all my skills & knowledge which would help the organization to grow & further enhance my growth profile. It would be my never-ending dedication to maintain the spectrum of integrity‚ honesty& character. Education qualification: degree M.pharm B.pharm Xll X
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…………………………………………………………………………….17 EFAS Matrix Analysis ……………………………………………………………………….. 18 Introduction Global pharmaceuticals grew by 3.6% in 2010 to reach over $733 billion with projections reaching $981 billion by the year 2015 (Pharmaceuticals Industry Profile: Global‚ 2011). Pfizer‚ the world leader in the global pharmaceuticals market‚ controls an impressive 9.4% of the global market share (Pharmaceuticals Industry Profile: Global‚ 2011). Sometimes described as Frankenstein’s Monster‚ Pfizer has been aggressively
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PROJECT REPORT ON A Successful International Merger in India: GlaxoSmithKline pharmaceutical industry Table of Contents: Declaration Abstract Part I –Introduction Research Objective and justifications Report Outline Part-II Industry Description
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more than 50-fold overnight is defending his decision with assertions that the profits will help create better medicines in future. The Infectious Diseases Society of America and the HIV Medicine Association sent a joint‚ open letter to Turing Pharmaceuticals earlier in September‚ complaining that the sudden‚ steep price increase for Daraprim was “unjustifiable for the medically vulnerable patient population” and also that it was “unsustainable for the health care system. Shkreli said hiking the price
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each batch (see point #2). 2. Manufacturing Procedures: These should utilize pharmaceutical blending not paddle/ribbon blender-type mixers. In addition‚ contact the company to ask if they have a Certificate of Analysis (COA) on file‚ confirming the potency of each batch. If the company ignores you or hesitates‚ that’s not a good sign. Lastly‚ you should select a vitamin supplements maker that adheres to pharmaceutical GMP compliance - this is the
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INTRODUCTION Employee welfare means a planned programme of activities or schemes that lead to the benefits of employee‚ in practical sense the above meaning is not exhaustive. According to the report of the Royal Commission Labour‚ the term welfare as applied to the industrial worker is one which must necessarily provide and is having different interpretation in one country from another‚ according to the different social customs‚ the degree of industrialization and educational development of the
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Table of content Chapter Title Page 1.1 Introduction and background 3 1.2 Methodology 4 2.1 Key opportunities
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reviews the history of Cleaning Validation Acceptance Limits for Active Pharmaceutical Ingredients (APIs) and identifies where the currently used industry limits came from. Cleaning Validation for the 21st Century: Acceptance Limits for Active Pharmaceutical Ingredients (APIs): Part I by Andy Walsh P Introduction art I of this article reviews the history of Cleaning Validation Acceptance Limits for Active Pharmaceutical Ingredients (APIs) and identifies the origins of currently used industry
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