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Titlebook: Bioequivalence Requirements in Various Global Jurisdictions; Isadore Kanfer Book 2017 American Association of Pharmaceutical Scientists 20

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樓主: Filament
11#
發(fā)表于 2025-3-23 10:33:18 | 只看該作者
Kundenorientierung im Kulturbetriebfied customs territory within the mutual trade in goods and does not apply customs duties and economic restrictions, except for special protective, antidumping and countervailing measures. The Republics of Belarus and Kazakhstan and the Russian Federation, in accordance with the Agreement of October
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發(fā)表于 2025-3-23 17:41:34 | 只看該作者
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發(fā)表于 2025-3-23 19:40:53 | 只看該作者
14#
發(fā)表于 2025-3-24 00:58:01 | 只看該作者
15#
發(fā)表于 2025-3-24 03:04:14 | 只看該作者
Forschungsmethodik und Aufbau der ArbeitThis chapter contains basically the same information as previously published [1]. Each law and/or regulation has been summarized more concisely. In addition, all new regulations approved after 2010 have been included, such as Resolution 37/11 and 27/12, dealing with biowaivers and bioanalytical method validation, respectively.
16#
發(fā)表于 2025-3-24 08:35:58 | 只看該作者
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發(fā)表于 2025-3-24 12:02:46 | 只看該作者
18#
發(fā)表于 2025-3-24 16:01:44 | 只看該作者
China,In 2010, China emerged as the fifth largest world pharmaceutical market and is projected to become the third largest market by 2020. China’s position as a force in the globalization of drug development became evident in the past few years.
19#
發(fā)表于 2025-3-24 21:17:53 | 只看該作者
South Africa,f medicines and for an application to amend a registered medicine. The types of medicine include a new medical entity (NCE), multisource (generic) products, a product line extension and a biological medicine.
20#
發(fā)表于 2025-3-25 02:32:34 | 只看該作者
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