欢迎您注册蒲公英
您需要 登录 才可以下载或查看,没有帐号?立即注册
x
Self-Identification of Generic Drug Facilities, Sites, andOrganizations 仿制药设施、工厂和组织的自我识别 Guidance for Industry 行业指南 U.S. Department of Health and HumanServices Food and Drug Administration Center for Drug Evaluation and Research(CDER) Center for Biologics Evaluation andResearch (CBER) September 2016 Generics
I. INTRODUCTION | 概述 | II. BACKGROUND | 背景 | III. GDUFA SELF-IDENTIFICATION REQUIREMENTS | GDUFA自我识别要求 | A. Who Is Required to Self-Identify? | 谁要做自我识别? | B. What Information Is Required for Submission? | 要提交哪些信息? | 1. D-U-N-S Numbers | 邓白氏号 | 2. Facility Establishment Identifier | 工厂设施识别号 | 3. Additional Information | 其它信息 | C. What Is the Process for Submitting Self-Identification Information? | 提交自我识别信息流程如何? | D. What Is the Penalty for Failing to Self-Identify? | 不做自我识别有什么处罚? |
|