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Titlebook: Biomedical Product Development: Bench to Bedside; Babak Arjmand,Moloud Payab,Parisa Goodarzi Textbook 2020 Springer Nature Switzerland AG

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41#
發(fā)表于 2025-3-28 16:04:56 | 只看該作者
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發(fā)表于 2025-3-28 20:36:58 | 只看該作者
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發(fā)表于 2025-3-29 00:59:10 | 只看該作者
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發(fā)表于 2025-3-29 05:54:19 | 只看該作者
45#
發(fā)表于 2025-3-29 07:32:33 | 只看該作者
Principles of Good Laboratory Practice (GLP),l risk management. Moreover, it is important to know how scientists use quality setting to improve biological products and data. Finally, research authorities should prove that there are no changes in the quality of data [1, 3].
46#
發(fā)表于 2025-3-29 11:54:42 | 只看該作者
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發(fā)表于 2025-3-29 19:05:03 | 只看該作者
48#
發(fā)表于 2025-3-29 22:39:47 | 只看該作者
Principles of Good Laboratory Practice (GLP),ology laboratories and increase the number of laws for chemical and pharmaceutical products [1]. They discovered a lot of fraudulent activities and poor laboratory practices such as uncalibrated equipment, wrong measurements, inaccurate data, and inadequate test systems. Accordingly, by setting GLP
49#
發(fā)表于 2025-3-30 00:40:14 | 只看該作者
Design of Experimental Studies in Biomedical Sciences,fundamental importance. Well-designed experimental studies with considering key points which are appropriately analyzed and reported could maximize scientific gains. However, there are still some problems in this process that should be addressed. Accordingly, using adequate methods based on the aim
50#
發(fā)表于 2025-3-30 05:46:16 | 只看該作者
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