no20xiaoxiong 2021-08-15 16:48 IP:武汉
求购盐酸戊乙奎醚注射液质量标准pdf版,国药准字H20193271、国药准字H20203005、国药准字H20203004、国药准字H20203003的质量标准,不必四个都要。   [更多]
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luojunwei2018 2021-01-12 11:25 IP:吉安
1.上市许可持有人(委托生产)生产许可证(B证)的MAH质量管理体系全套文件及文件目录 2.要求2020年11月后通过生产许可证检查的全套文件,价格可以协商 。 3.包含四大体系文件。   [更多]
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zhangxue521 2021-01-15 15:39 IP:广州
求购氨溴特罗口服溶液质量标准或者最新的注册标准   [更多]
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StevenChow 2015-07-17 15:49 IP:无锡
详细要求:江苏红豆杉药业有限公司接受抗肿瘤药的委托生产,拥有小容量注射剂(非最终灭菌、抗肿瘤药)、冻干粉(抗肿瘤药)的生产线,寻找没有生产线需要委托生产、中试放大生产的公司。 具体要求:提供需要委托生产的公司名称、联系人、联系方式,并最终合作成功。 交稿方式:直接点击交稿在线交稿就是了,我会每天过来看的,谢谢各位药智的战友们   [更多]
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wangrong 2023-05-29 14:10 IP:未知
左卡尼汀注射液   过评质量信息   [更多]
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xiaoliwugang 2018-08-07 15:34 IP:上海
产品:间苯三酚口服冻干片(Spasfon-Lyoc) 厂家:TEVA 上市国家:法国 具体的冻干工艺和处方   [更多]
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jimw0511 2021-06-10 13:52 IP:北京
东莨菪碱贴片(可弥特) 【英 文 名】 Scopolamine Patch(Kimite) 【生产厂商】 韩国 MyungMoon Pharmaceutial Co.,Ltd. 【 规 格 】 0.75mg、1.5mg 【注册证号】 H20040569、H20040570 【标 准 号】 JX20010447   [更多]
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nongzr123456 2023-02-27 10:15 IP:广州
求购地夸磷索钠原料药质量信息(原研,清晰电子版)   [更多]
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qiyan_xiao 2022-11-03 16:04 IP:广州
2,6-二甲基苯胺作为基因毒性杂质控制,它的每日最大摄入量是多少?(1.5μg/天做不到)目前找到一个雷诺嗪缓释片在澳洲申报的资料中提到2,6-二甲基苯胺的每日最大摄入量范围是20.4μg/天~110μg/天,有没有哪位大神知道这两个值的来源及推导过程,求助。原文如下:The sponsor also commissioned two nonclinical risk assessments on DMA relative to  potential exposure from ranolazine under the conditions of use. Both assessors referred to  methodologies advocated in the ICH guideline.21 The updated guideline permits the use of  compound-specific assessments (compared with. TTC-based acceptable intake of  1.5 μg/day) when sufficient carcinogenicity data exists, such that a compound-specific  acceptable intake can be extrapolated from measures of carcinogenic potency. Information  on the carcinogenicity of DMA is available from a 2 year dietary study in rats (NTP, 1990)  and is the only source of data on carcinogenic potency. The first nonclinical assessor referred to a follow-up report to the NTP report where  carcinogenic potential (TD50) was set at 20.4 mg/kg. By linear extrapolation the  acceptable lifetime daily intake was calculated as 0.41 μg/kg/day (24.5 μg/day for 60 kg  adult or 20.4 μg/day for 50 kg adult). The amount of DMA detected in 750 mg ranolazine  tablets after 24 months storage (1.6 μg/tablet or 3.2 μg/day based on average batch values  outlined above in Table 7) were at least 6.4 fold lower than the extrapolated acceptable  lifetime daily intake of 20.4 μg/day (for 50 kg adult at the MRHD). The assessor indicated  that this was an acceptable safety factor but recommended that the shelf life of Ranexa be  no more than 24 months to ensure ranolazine degradation was minimal. The second nonclinical assessor evaluated risk assessments conducted by other regulatory  bodies where acceptable daily levels of DMA ranged between 20.4 μg/day to 110 μg/day  (for 50 kg adult). The most conservative approach gave acceptable daily levels of  29 μg/day (20.4 μg/day for 50 kg adult) and was the same as that   [更多]
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药丸199811 2023-09-18 10:11 IP:XX
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