蒋千琴

蒋千琴

FDA外审顾问

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以下是作者 蒋千琴 的最新文章

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  • FDA CVM GFI #132 Administrative Applications and the Phased Review Process

    FDA CVM GFI #132 Administrative Applications and the Phased Review Process

    CVM GFI #132 Administrative Applications and the Phased Review Process[附网盘链接]是Food And Drug Administration于不久之前发布的FDA标准，适用于US。本次分享的标准文档为高清PDF（文字版），标准文档内可搜索，可复制，可粘贴。本文结尾附网盘链接。

    1/20/2022 点赞 0 浏览 277 评论 0
  • FDA CVM GFI #108 Registering with CVM’s Electronic Submission System

    FDA CVM GFI #108 Registering with CVM’s Electronic Submission System

    CVM GFI #108 Registering with CVM’s Electronic Submission System[附网盘链接]是Food&Drug Administration于当前发布的FDA标准，适用于U.S。本次分享的标准文档为高清PDF（文字版），标准文档内可搜索，可复制，可粘贴。本文结尾附网盘链接。

    1/19/2022 点赞 0 浏览 239 评论 0
  • FDA CVM GFI #118 Mass Spectrometry for Confirmation of Identity of Animal Drug Residues

    FDA CVM GFI #118 Mass Spectrometry for Confirmation of Identity of Animal Drug Residues

    CVM GFI #118 Mass Spectrometry for Confirmation of Identity of Animal Drug Residues[附网盘链接]是Food&Drug Administration于不久前发布的FDA标准，适用于美国。本次分享的标准文档为高清PDF（文字版），标准文档内可搜索，可复制，可粘贴。本文结尾附网盘链接。

    1/19/2022 点赞 0 浏览 240 评论 0
  • FDA Cutaneous Electrodes for Recording Purposes - Performance Criteria for Safety and Performance Based Pathway

    FDA Cutaneous Electrodes for Recording Purposes - Performance Criteria for Safety and Performance Based Pathway

    Cutaneous Electrodes for Recording Purposes - Performance Criteria for Safety and Performance Based Pathway[附网盘链接]是Food And Drug Administration于不久之前发布的FDA标准，适用于US。本次分享的标准文档为高清PDF（文字版），标准文档内可搜索，可复制，可粘贴。本文结尾附网盘链接。

    1/18/2022 点赞 0 浏览 281 评论 0
  • FDA CVM GFI #100 (VICH GL18) Residual Solvents in New Veterinary Medicinal Products

    FDA CVM GFI #100 (VICH GL18) Residual Solvents in New Veterinary Medicinal Products

    CVM GFI #100 (VICH GL18) Residual Solvents in New Veterinary Medicinal Products[附网盘链接]是Food&Drug Administration于之前发布的FDA标准，适用于美国。本次分享的标准文档为高清PDF（文字版），标准文档内可搜索，可复制，可粘贴。本文结尾附网盘链接。

    1/18/2022 点赞 0 浏览 246 评论 0
  • FDA Current Good Manufacturing Practice—Human Drug Compounding Outsourcing Facilities Under Section 503B of the FD&C Act

    FDA Current Good Manufacturing Practice—Human Drug Compounding Outsourcing Facilities Under Section 503B of the FD&C Act

    Current Good Manufacturing Practice—Human Drug Compounding Outsourcing Facilities Under Section 503B of the FD&C Act[附网盘链接]是Food And Drug Administration于不久前发布的FDA标准，适用于U.S。本次分享的标准文档为高清PDF（文字版），标准文档内可搜索，可复制，可粘贴。本文结尾附网盘链接。

    1/17/2022 点赞 0 浏览 231 评论 0
  • FDA Custom Device Exemption Guidance for Industry and Food and Drug Administration Staff

    FDA Custom Device Exemption Guidance for Industry and Food and Drug Administration Staff

    Custom Device Exemption Guidance for Industry and Food and Drug Administration Staff[附网盘链接]是Food And Drug Administration于不久之前发布的FDA标准，适用于U.S。本次分享的标准文档为高清PDF（文字版），标准文档内可搜索，可复制，可粘贴。本文结尾附网盘链接。

    1/17/2022 点赞 0 浏览 240 评论 0
  • FDA Current Good Manufacturing Practice for Medical Gases Draft Guidance for Industry

    FDA Current Good Manufacturing Practice for Medical Gases Draft Guidance for Industry

    Current Good Manufacturing Practice for Medical Gases Draft Guidance for Industry[附网盘链接]是Food&Drug Administration于之前发布的FDA标准，适用于US。本次分享的标准文档为高清PDF（文字版），标准文档内可搜索，可复制，可粘贴。本文结尾附网盘链接。

    1/16/2022 点赞 0 浏览 167 评论 0
  • FDA Cross Labeling Oncology Drugs in Combination Regimens Guidance for Industry Draft

    FDA Cross Labeling Oncology Drugs in Combination Regimens Guidance for Industry Draft

    Cross Labeling Oncology Drugs in Combination Regimens Guidance for Industry Draft[附网盘链接]是FDA于过去发布的FDA标准，适用于美国。本次分享的标准文档为高清PDF（文字版），标准文档内可搜索，可复制，可粘贴。本文结尾附网盘链接。

    1/16/2022 点赞 0 浏览 236 评论 0
  • FDA Critical Path Innovation Meetings

    FDA Critical Path Innovation Meetings

    Critical Path Innovation Meetings[附网盘链接]是Food And Drug Administration于不久之前发布的FDA标准，适用于United States。本次分享的标准文档为高清PDF（文字版），标准文档内可搜索，可复制，可粘贴。本文结尾附网盘链接。

    1/15/2022 点赞 0 浏览 127 评论 0
  • FDA CPG Sec. 683.100 Action Levels for Aflatoxins in Animal Feeds

    FDA CPG Sec. 683.100 Action Levels for Aflatoxins in Animal Feeds

    CPG Sec. 683.100 Action Levels for Aflatoxins in Animal Feeds[附网盘链接]是Food&Drug Administration于之前发布的FDA标准，适用于美国。本次分享的标准文档为高清PDF（文字版），标准文档内可搜索，可复制，可粘贴。本文结尾附网盘链接。

    1/15/2022 点赞 0 浏览 202 评论 0
  • FDA CPG Sec. 665.300 Use of Type A Medicated Article Proprietary Names in the Names of Medicated Feeds

    FDA CPG Sec. 665.300 Use of Type A Medicated Article Proprietary Names in the Names of Medicated Feeds

    CPG Sec. 665.300 Use of Type A Medicated Article Proprietary Names in the Names of Medicated Feeds[附网盘链接]是Food&Drug Administration于之前发布的FDA标准，适用于美国。本次分享的标准文档为高清PDF（文字版），标准文档内可搜索，可复制，可粘贴。本文结尾附网盘链接。

    1/14/2022 点赞 0 浏览 217 评论 0
  • FDA CPG Sec. 666.100 Alternate Feeding of Different Medicated Feeds

    FDA CPG Sec. 666.100 Alternate Feeding of Different Medicated Feeds

    CPG Sec. 666.100 Alternate Feeding of Different Medicated Feeds[附网盘链接]是Food And Drug Administration于当前发布的FDA标准，适用于United States。本次分享的标准文档为高清PDF（文字版），标准文档内可搜索，可复制，可粘贴。本文结尾附网盘链接。

    1/14/2022 点赞 0 浏览 213 评论 0
  • FDA CPG Sec. 653.100 Animal Grooming Aids

    FDA CPG Sec. 653.100 Animal Grooming Aids

    CPG Sec. 653.100 Animal Grooming Aids[附网盘链接]是Food And Drug Administration于不久前发布的FDA标准，适用于U.S。本次分享的标准文档为高清PDF（文字版），标准文档内可搜索，可复制，可粘贴。本文结尾附网盘链接。

    1/13/2022 点赞 0 浏览 314 评论 0
  • FDA CPG Sec. 651.100 Ethylenediamine Dihydroiodide (EDDI)

    FDA CPG Sec. 651.100 Ethylenediamine Dihydroiodide (EDDI)

    CPG Sec. 651.100 Ethylenediamine Dihydroiodide (EDDI)[附网盘链接]是Food&Drug Administration于当前发布的FDA标准，适用于U.S。本次分享的标准文档为高清PDF（文字版），标准文档内可搜索，可复制，可粘贴。本文结尾附网盘链接。

    1/13/2022 点赞 0 浏览 183 评论 0