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Titlebook: Quick Guide to Good Clinical Practice; How to Meet Internat Cemal Cingi,Nuray Bayar Muluk Book 2017 Springer International Publishing Switz

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樓主: 審美家
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發(fā)表于 2025-3-30 10:00:48 | 只看該作者
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發(fā)表于 2025-3-30 15:59:25 | 只看該作者
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發(fā)表于 2025-3-30 17:15:12 | 只看該作者
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發(fā)表于 2025-3-30 21:02:30 | 只看該作者
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發(fā)表于 2025-3-31 04:42:29 | 只看該作者
The Drug Development Process and Evolution of Regulations, to less than one in two [1, 2]. Less than 20 % of drugs entering phase-1 testing successfully reach the end of the three-phase evaluation. The percentage can vary from one specialty area to another and can be less than 5–10 % for oncologic and neurologic diseases [3].
56#
發(fā)表于 2025-3-31 09:02:52 | 只看該作者
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發(fā)表于 2025-3-31 09:56:01 | 只看該作者
The Definition of GCP,ant scientific and healthcare questions. Randomised controlled trials form the foundation for ‘evidence-based medicine’, but such research can be relied upon only if it is conducted according to principles and standards collectively referred to as ‘good clinical research practice’ (GCP) [1].
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發(fā)表于 2025-3-31 13:24:10 | 只看該作者
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發(fā)表于 2025-3-31 18:52:23 | 只看該作者
Setting the Ideal Method,ion, we need to consider the best strategy to address these questions. Further considerations in clinical research, such as the clinical setting, study design, selection criteria, data collection and analysis, are influenced by the disease characteristics, prevalence, time availability, expertise, research grants and several other factors [1].
60#
發(fā)表于 2025-3-31 23:32:43 | 只看該作者
Book 2017l quality standard – Good Clinical Practice – provided by the International Conference on Harmonization (ICH).?.The work offers an updated perspective on the clinical research landscape within the context of the clinical trial regulatory frameworks in Europe and the USA. In addition to providing a h
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