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標題: Titlebook: Bioequivalence Requirements in Various Global Jurisdictions; Isadore Kanfer Book 2017 American Association of Pharmaceutical Scientists 20 [打印本頁]

作者: Filament    時間: 2025-3-21 16:45
書目名稱Bioequivalence Requirements in Various Global Jurisdictions影響因子(影響力)




書目名稱Bioequivalence Requirements in Various Global Jurisdictions影響因子(影響力)學科排名




書目名稱Bioequivalence Requirements in Various Global Jurisdictions網絡公開度




書目名稱Bioequivalence Requirements in Various Global Jurisdictions網絡公開度學科排名




書目名稱Bioequivalence Requirements in Various Global Jurisdictions被引頻次




書目名稱Bioequivalence Requirements in Various Global Jurisdictions被引頻次學科排名




書目名稱Bioequivalence Requirements in Various Global Jurisdictions年度引用




書目名稱Bioequivalence Requirements in Various Global Jurisdictions年度引用學科排名




書目名稱Bioequivalence Requirements in Various Global Jurisdictions讀者反饋




書目名稱Bioequivalence Requirements in Various Global Jurisdictions讀者反饋學科排名





作者: nonchalance    時間: 2025-3-21 20:13
Verkaufsf?rderung im Kulturbereichto which the . bioequivalence (reference standard) and, in some instances, the . bioequivalence of the applicant’s product is compared are listed by the US-FDA in its publication . (the Orange Book). The Orange Book identifies all prescription and over-the-counter (OTC) drug products approved for ma
作者: 種子    時間: 2025-3-22 03:21

作者: 我悲傷    時間: 2025-3-22 07:23

作者: PON    時間: 2025-3-22 11:49
Bioequivalence Requirements in Various Global Jurisdictions
作者: Airtight    時間: 2025-3-22 14:01

作者: Optic-Disk    時間: 2025-3-22 18:06
,Theoriebezüge zur Kundenauswahl,rding to IMS Health, GDPs are expected to account for 52% of global pharmaceutical spending in 2018 compared to 35% for branded drug products [2]. Moreover, the impact of GDPs on drug spending will make even more impact in the coming years, resulting from the fact that small molecule patent expirati
作者: 防止    時間: 2025-3-22 21:48
,Theoriebezüge zur Kundenauswahl,ucts, chlorpromazine, digitoxin, digoxin, lithium carbonate, quinidine, tetracycline, and tolbutamide in the Indian Pharmacopoeia in 1985, [1] initiated the process of framing legislation for regulatory requirements of BE studies. After this phase (3?years), BE studies became mandatory for all new d
作者: Senescent    時間: 2025-3-23 03:54

作者: ACME    時間: 2025-3-23 06:22
https://doi.org/10.1007/978-3-322-81424-1cal Industry-League of Arab States in 2014. The new guidance has been approved by health regulatory authorities’ representatives from MENA Region including Kingdom of Saudi Arabia, Kingdom of Jordan, Republic of Sudan, Republic of Algeria, Republic of Libya, Republic of Iraq, Republic of Egypt, Sult
作者: 原諒    時間: 2025-3-23 10:33
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
作者: ORE    時間: 2025-3-23 17:41

作者: 鉗子    時間: 2025-3-23 19:40

作者: freight    時間: 2025-3-24 00:58

作者: 籠子    時間: 2025-3-24 03:04
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.
作者: –LOUS    時間: 2025-3-24 08:35

作者: commute    時間: 2025-3-24 12:02

作者: Obstruction    時間: 2025-3-24 16:01
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.
作者: 消滅    時間: 2025-3-24 21:17
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.
作者: 開始發(fā)作    時間: 2025-3-25 02:32

作者: 兵團    時間: 2025-3-25 06:51

作者: foliage    時間: 2025-3-25 10:59

作者: 直覺沒有    時間: 2025-3-25 13:21
AAPS Advances in the Pharmaceutical Sciences Serieshttp://image.papertrans.cn/b/image/186927.jpg
作者: Perigee    時間: 2025-3-25 17:36

作者: 壯麗的去    時間: 2025-3-25 20:29
978-3-319-88542-1American Association of Pharmaceutical Scientists 2017
作者: Demulcent    時間: 2025-3-26 00:58

作者: Commodious    時間: 2025-3-26 07:11

作者: 使厭惡    時間: 2025-3-26 10:42

作者: FRONT    時間: 2025-3-26 13:11

作者: avenge    時間: 2025-3-26 18:13
Kundenorientierung im Kulturbetriebection with this Agreement which contains an approach to prepare a unified guidance for BE studies, a plan for document preparation has been approved (a Custom Union BE guidance was approved in May 2017).
作者: FRAUD    時間: 2025-3-27 00:03

作者: multiply    時間: 2025-3-27 02:30

作者: Peristalsis    時間: 2025-3-27 05:59
The European Union,ribution than in the past 5?years, and no single year will reach the level seen in 2012. Generic medicines will continue to provide the vast majority of the prescription medicines use in the US, rising from 88% to over 90% of all dispensed prescriptions by 2020 [2].
作者: 一條卷發(fā)    時間: 2025-3-27 13:04
Russia, Belarus & Kazakhstan,ection with this Agreement which contains an approach to prepare a unified guidance for BE studies, a plan for document preparation has been approved (a Custom Union BE guidance was approved in May 2017).
作者: blithe    時間: 2025-3-27 15:25
World Health Organisation (WHO), enjoy political support for the regulators, or have properly resourced and functioning regulatory authorities [2]. It is no wonder that in many resource-poor settings patients do not trust locally authorized multisource (generic) products.
作者: 條街道往前推    時間: 2025-3-27 21:19

作者: Orgasm    時間: 2025-3-28 01:01

作者: cortex    時間: 2025-3-28 05:55

作者: Toxoid-Vaccines    時間: 2025-3-28 08:58
Japan, These figures pale in comparison with countries such as the United States, Germany, and the United Kingdom where generic drug product penetration levels are far more than half of the total pharmaceutical products volume.
作者: absorbed    時間: 2025-3-28 13:04

作者: 剛毅    時間: 2025-3-28 15:45
,Theoriebezüge zur Kundenauswahl,rugs introduced on the markets in India, by incorporating Schedule Y of the Drugs and Cosmetics Act in 1988, followed by subsequent amendments of Schedule Y in 1989 and 2005 [2]. The term “new drug” in India is defined on page 3 as follows,
作者: tariff    時間: 2025-3-28 18:55

作者: 驕傲    時間: 2025-3-29 00:45

作者: 琺瑯    時間: 2025-3-29 06:51

作者: 面包屑    時間: 2025-3-29 08:44

作者: 沉思的魚    時間: 2025-3-29 13:37

作者: 避開    時間: 2025-3-29 16:01
Russia, Belarus & Kazakhstan,fied 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
作者: COWER    時間: 2025-3-29 21:31

作者: 反省    時間: 2025-3-29 23:53

作者: 文藝    時間: 2025-3-30 07:15

作者: Solace    時間: 2025-3-30 08:26
10樓
作者: 小步走路    時間: 2025-3-30 14:15
10樓
作者: 不開心    時間: 2025-3-30 19:15
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