標(biāo)題: Titlebook: Regulation of the Pharmaceutical Industry; John Abraham (Professor of Sociology and Co-direct Book 2003 Palgrave Macmillan, a division of [打印本頁] 作者: 大小 時間: 2025-3-21 18:25
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作者: 起波瀾 時間: 2025-3-21 20:47 作者: 高射炮 時間: 2025-3-22 04:06 作者: 上下倒置 時間: 2025-3-22 07:35
Eeva Ollila,Elina Hemminkiman Rights. The historical roots of the two systems are briefly outlined. In this historical development, it is noted that the confession has full centuries been regarded as a gold standard of proof. This old certainty is now being questioned, particularly in the light of psychological investigation作者: 花束 時間: 2025-3-22 09:35
Norma Morriships, case review and broadening the perspective from a particular professional standpoint alone, improvement in continuity of care, promotion of sharing of information on a proportional basis and shared educational opportunities. Potential disadvantages include breach of confidentiality, continued 作者: 假設(shè) 時間: 2025-3-22 16:58
Toine Pietersand it is arguable that the most important resolution lies in clarity for all parties on the nature and extent of roles and relationships. We go on to show that, even within an inquisitorial approach, there needs to be no strict separation between evaluation for legal purposes and therapy, using the作者: Polydipsia 時間: 2025-3-22 21:04
Jessika Van Kammenealth and Justice TBS system or prison hospital units. In Finland and the UK, inpatient services are all health service based and clinical input to prisons by health service employees only. Development of offender pathway maps is likely to assist mutual understanding of services. They could be used 作者: certitude 時間: 2025-3-23 00:57 作者: 呼吸 時間: 2025-3-23 02:57 作者: 實(shí)施生效 時間: 2025-3-23 05:50 作者: HAVOC 時間: 2025-3-23 13:10 作者: CURT 時間: 2025-3-23 15:32
Regulatory Laws and Political Culture in the United States and Germany,rstanding differences in cultures of testing and regulation is essential to crafting productive systems for medical innovation and will be crucial to current efforts at international harmonization across Europe, the United States, and Japan (Abraham, 1997; Kidd, 1996).作者: 整潔 時間: 2025-3-23 18:39 作者: 半球 時間: 2025-3-23 23:09
John Abrahamand analysis. It also discusses forensic gate and analysis as well as the identification of pedal remains from podiatry records, which is important for mass disaster scenes. Part III978-1-62703-821-8978-1-61737-976-5作者: 描述 時間: 2025-3-24 06:12
Arthur Daemmrichand analysis. It also discusses forensic gate and analysis as well as the identification of pedal remains from podiatry records, which is important for mass disaster scenes. Part III978-1-62703-821-8978-1-61737-976-5作者: Substitution 時間: 2025-3-24 10:12
Book 2003ned by scientific experts, a democratic state, the interests of final users, or ethical principles? This unique collection brings together the work of social scientists, ethicists, lawyers and policy analysts on regulation, ethics and innovation in the pharmaceutical industry. Regulatory systems and作者: 免費(fèi) 時間: 2025-3-24 10:56 作者: transient-pain 時間: 2025-3-24 15:58
Globalization of Medicines Control,s and regulation across regions of the world. However, those who are skeptical about whether globalization is occurring argue that there is insufficient detailed empirical evidence demonstrating such a process (Busch, 2000).作者: 遺忘 時間: 2025-3-24 21:41 作者: vitreous-humor 時間: 2025-3-24 23:42
Book 2003 social scientists, ethicists, lawyers and policy analysts on regulation, ethics and innovation in the pharmaceutical industry. Regulatory systems and their implications for public health in North America, Europe and developing countries are discussed, including case studies of norplant, interferon and anti-fertility vaccines.作者: Ornament 時間: 2025-3-25 07:07
Europeanization of Medicines Regulation, the relevant EU organizations, conducted between 1994 and 1998. In particular we focus on the politics of scientific expertise within the Europeanization process and the implications of the latter for drug safety, public health and the democratic accountability of regulatory decision making.作者: barium-study 時間: 2025-3-25 07:44
Sales Licensing Documentation and Trade Secrecy: the case of NorplantR Contraceptives,ortant form of public regulation on drugs. Based on the information provided by the product license holder, the drug regulatory authorities evaluate the risks and benefits of the drug during the sales licensing process to determine whether the drug should be allowed to enter the markets of that country.作者: Anterior 時間: 2025-3-25 14:37
2947-3829 be determined by scientific experts, a democratic state, the interests of final users, or ethical principles? This unique collection brings together the work of social scientists, ethicists, lawyers and policy analysts on regulation, ethics and innovation in the pharmaceutical industry. Regulatory s作者: 外貌 時間: 2025-3-25 17:48 作者: Irrigate 時間: 2025-3-25 20:55 作者: 雪白 時間: 2025-3-26 01:00
The Limitations of Current Ethical Regulations,ncipatory status. I draw upon a number of studies to illustrate the effects of the implementation of informed consent in various social contexts. Finally, I argue the central role accorded to informed consent obfuscates other ethical issues relating to the broader political and institutional setting作者: 絕緣 時間: 2025-3-26 07:55 作者: Foregery 時間: 2025-3-26 10:58
Introduction,rmaceutical industry’ and ‘regulation’. This is not entirely straightforward because regulation shapes the industry and vice-versa. In some contexts, technological innovations may drive the construction of regulations and governance. For this reason it is important to examine the process of pharmace作者: overwrought 時間: 2025-3-26 12:55 作者: Chromatic 時間: 2025-3-26 17:52 作者: nettle 時間: 2025-3-26 23:52 作者: 擺動 時間: 2025-3-27 05:00
Sales Licensing Documentation and Trade Secrecy: the case of NorplantR Contraceptives,quality and rationally used. Vital drugs should be available and accessible at a reasonable cost for the individual and for the society. Rational use of drugs implies that, in addition to the properties of the drugs, there is adequate information to select the most appropriate drug or no drug at all作者: 數(shù)量 時間: 2025-3-27 05:37
Biological Medicines in the Age of Biotech: Public Policy Issues,class of medicines known as ‘biologicals’. Take, for example, blood and blood products. They are an essential and life-saving component of everyday medical practice. But the AIDS epidemic provided painful evidence of how disease could be transmitted by donated blood or products made from it, such as作者: ingestion 時間: 2025-3-27 09:39 作者: Cpap155 時間: 2025-3-27 15:56 作者: 保守 時間: 2025-3-27 18:54
Regulation for Ethical Purposes: Medical Research on Humans,ich began as very unregulated regulators and have become highly regulatory and increasingly regulated themselves. I conclude with some reflections on future developments, taking the draft European Directive on clinical trials into account.作者: 松馳 時間: 2025-3-28 01:25
The Limitations of Current Ethical Regulations,rug trials in particular. The principle of informed consent, is central to these guidelines and has come to be seen as ‘the ethical solution’ to prevent the exploitation and abuse of human subjects. I present a critical examination of the central role accorded to this principle and challenge its ema作者: 執(zhí) 時間: 2025-3-28 05:37
Mergers and Joint Ventures in the Pharmaceutical Industry,s have had on the treatment of all joint ventures including those in the pharmaceutical industry. It also provides some insight into the way in which the European Commission and the UK competition authorities are likely to approach the definition of relevant markets in future mergers and joint ventu作者: PANIC 時間: 2025-3-28 08:48 作者: bypass 時間: 2025-3-28 14:23 作者: escalate 時間: 2025-3-28 14:39 作者: Brittle 時間: 2025-3-28 21:26 作者: 個阿姨勾引你 時間: 2025-3-28 23:50 作者: stratum-corneum 時間: 2025-3-29 05:32 作者: 兇猛 時間: 2025-3-29 09:36
