ccn13831117235 2022-05-13 13:16 IP:石家庄
一类医疗器械《一次性使用引流袋》注册资料(全套资料   [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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s18220376932 2023-03-01 15:57 IP:XX
混悬型乳膏剂;要全套的注册申报资料模板(数据等需要保密的可删);   [更多]
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oogxoo 2023-09-18 17:04 IP:未知
执行标准JX20220120或其他标准亦可   [更多]
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张新春newyear 2018-05-08 21:57 IP:南京
需要碘克沙醇注射液说明书,北京北陆和扬子江的。清晰,拍照即可。联系13764673863   [更多]
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lskingzctx 2022-11-09 15:15 IP:成都
设备、工艺相关资料。资料合适可议价。   [更多]
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HZCCY1024 2020-06-06 09:25 IP:重庆
1、文件包括质量手册、程序文件、管理制度、SOP和表单,文件应齐全,医疗器械临床试验的优先。 2、体系文件能够指导临床试验的开展。   [更多]
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塔桥 2023-10-08 08:37 IP:南京
求购克立硼罗软膏参比厂家的产品开发过程信息(P.2)或稳定性信息(P.8)   [更多]
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lxw1987 2021-09-07 15:10 IP:成都
包括:所有检测项以及内容,其中有关物质必须有检测方法,杂质控制及限度。   [更多]
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Kutter 2022-08-18 07:40 IP:德阳
至少包括3.2.P.2 3.2.P.3 3.2.P.5   [更多]
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