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Volumn 8, Issue 3, 2007, Pages 9-16

What will pharma look like in 2020?

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; DRUG INDUSTRY; DRUG MARKETING; DRUG RESEARCH; FINANCIAL MANAGEMENT; GOVERNMENT REGULATION; HEALTH CARE MANAGEMENT; HEALTH INSURANCE; MEDICAL PRACTICE; PRESCRIPTION; PRODUCT DEVELOPMENT;

EID: 34547531474     PISSN: 14694344     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (1)

References (18)
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    • In 2006, the member companies of Pharmaceutical Research and Manufacturers of America spent $43 billion on R&D, nearly three times the $15.2 billion they spent on R&D in 1995, and more than twice the $19.84 billion this sum would now be worth when adjusted for inflation. However, the US Food and Drug Administration approved only 22 new molecular entities in 2006, compared with the 53 it approved in 1995
    • In 2006, the member companies of Pharmaceutical Research and Manufacturers of America spent $43 billion on R&D - nearly three times the $15.2 billion they spent on R&D in 1995, and more than twice the $19.84 billion this sum would now be worth when adjusted for inflation. However, the US Food and Drug Administration approved only 22 new molecular entities in 2006, compared with the 53 it approved in 1995.
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    • Impact of Regulation on the Uptake and Diffusion of Pharmaceutical Innovations: Systematic Review
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  • 5
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    • In a survey of the attitudes of oncologists by Dr Eric Nadler, a researcher at Harvard Medical School, about 80% of the respondents said that they would prescribe a drug costing up to $70,000, even if it could only extend a patienes life by two months more than the standard treatment. For further information, see Alex Berenson, Cancer Drugs Offer Hope, but at a Huge Expense, The New York Times July 12, 2005, accessed April 26, 2007
    • In a survey of the attitudes of oncologists by Dr Eric Nadler, a researcher at Harvard Medical School, about 80% of the respondents said that they would prescribe a drug costing up to $70,000, even if it could only extend a patienes life by two months more than the standard treatment. For further information, see Alex Berenson, "Cancer Drugs Offer Hope, but at a Huge Expense", The New York Times (July 12, 2005), accessed April 26, 2007, http://www.nytimes.com/2005/07/12/ business/12cancer.html?ex=1278820800&en=1eb889752ca5eb49&ei= 5088&partner=rssnyt&emc=rss.
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    • The Centers for Medicare and Medicaid Services reports that the US spent $1.99 trillion on healthcare in 2005, and that $200.7 billion went on prescription drugs. Information accessed April 26, 2007, http://www.cms.hhs.gov/NationalHealthExpendData/ 02_NationalHealthAccountsHistorical.asp#TopOfPage.
    • The Centers for Medicare and Medicaid Services reports that the US spent $1.99 trillion on healthcare in 2005, and that $200.7 billion went on prescription drugs. Information accessed April 26, 2007, http://www.cms.hhs.gov/NationalHealthExpendData/ 02_NationalHealthAccountsHistorical.asp#TopOfPage.
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    • Australia, Belgium, Canada, Cuba, England, France, Hong Kong, India, Ireland, Italy, Montenegro, New Zealand, Norway, Scotland, Sweden, Singapore, Uruguay and Wales have introduced nationwide bans on smoking in enclosed public places. A number of US states have introduced similar rules. For further information, see BBC News, "Smoking curbs:The global picture" Oanuary 31, 2007), accessed April 26, 2007, http://news.bbc.co.uk/1/hi/world/3758707.stm.
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    • Drugs, devices, and the promise of pervasive computing
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    • In-life testing is the use of remote monitoring devices to track how patients respond to medicines in a real-life setting rather than the rarefied environment of clinical trials. This concept was first articulated in the IBM Global Business Services paper Pharma 2010: The threshold of innovation (2002), accessed April 26, 2007, http://www-935.ibm.com/services/de/bcs/pdf/2006/pharma_2010.pdf.
    • "In-life testing" is the use of remote monitoring devices to track how patients respond to medicines in a real-life setting rather than the rarefied environment of clinical trials. This concept was first articulated in the IBM Global Business Services paper "Pharma 2010: The threshold of innovation" (2002), accessed April 26, 2007, http://www-935.ibm.com/services/de/bcs/pdf/2006/pharma_2010.pdf.
  • 17
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    • The European Medicines Agency authorised the use of conditional approvals for orphan drugs and therapies for life-threatening conditions in April 2006 under Regulation EC 507/2006.The US Food and Drug Administration is piloting the concept under the Prescription Drug User Fee Act (PDUFA) III
    • The European Medicines Agency authorised the use of conditional approvals for orphan drugs and therapies for life-threatening conditions in April 2006 under Regulation EC 507/2006.The US Food and Drug Administration is piloting the concept under the Prescription Drug User Fee Act (PDUFA) III.
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    • Health at a Glance
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.