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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与药共舞 2022-02-21 10:25 IP:合肥
求购注射用阿莫西林钠克拉维酸钾的注册质量标准,要求是2017年或之后的版本   [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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lihuan970108 2022-02-23 13:08 IP:北京
求购以下质量标准:脂肪乳氨基酸(17)葡萄糖(11%)注射液(卡文)执行质量标准(YBH00952017);脂肪乳氨基酸(17)葡萄糖(11%)注射液(卡文)注册标准;脂肪乳(10%)氨基酸(15)葡萄糖(20%)注射液注册标准;氨基酸葡萄糖注射液(克灵麦)注册标准(需要除JX20040105外的其余最新标准);氨基酸葡萄糖注射液(克灵麦)注册标准。   [更多]
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h670835911 2023-09-20 13:51 IP:未知
YBH00332021  或YBH02572020  或YBH00982021 或其他厂家过评标准提供一家即可   [更多]
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qh5018787 2022-02-24 11:30 IP:南京
 3.医疗器械安全有效基本要求清单 4.综述资料 5.研究资料 6.生产制造信息 7.临床评价资料 8.产品风险分析资料 9.产品技术要求 10.产品注册检验报告 11.说明书和标签样稿 12.符合性声明   [更多]
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hejiao 2015-08-25 09:10 IP:重庆
具体要求: 1、必须是儿科类的品种 2、剂型是口服液(片剂也能接受) 3、具备有效生产批件和新药证书,或者是国内独家品种。 4、要求直接提供项目所有者的联系方式,提供的信息真实有效。   [更多]
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