PART111第111CURRENTGOODMANUFACTURINGPRACTICEINMANUFACTURING, PACKAGING,LABELING,ORHOLDINGOPERATIONSFORDIETARYSUPPLEMENTS现行良好操 作规范在制造,包装,标签,或对食品补充剂控股作业SubpartA--General Provisions子部分-一般规定 Sec.秒。111.1Whoi
美国良好操作规范(GMP—21CFR Part 111).doc,[联邦法规] [Title 21, Volume 2] [标题21,第2卷] [Revised as of April 1, 2008] [日期为2008年4月1日] [CITE: 21CFR111] [引用:21CFR111] TITLE 21--FOOD AND DRUGS 标题21 -食品和药物 CHAPTER I--FOOD AND DRUG ADMINISTRA
[CITE: 21CFR111] [引用:21CFR111] TITLE 21--FOOD AND DRUGS标题21 -食品和药物 CHAPTER I--FOOD AND DRUG ADMINISTRATION第一章-食品和药物管理局 DEPARTMENT OF HEALTH AND HUMAN SERVICES部卫生与公众服务 SUBCHAPTER B--FOOD FOR HUMAN CONSUMPTION子章节B组-人类食用的食物 PART 111第111 CURRENT GOOD MA...
111 ⅠⅠⅠ 1-991-991-99 健康与人类服务部食品与药品管理局(健康与人类服务部食品与药品管理局(健康与人类服务部食品与药品管理局(FOODFOODFOOD ANDANDANDDRUGDRUGDRUGADMINISTRAADMINISTRAADMINISTRATION,TION,TION, DEPARTMENTDEPARTMENTDEPARTMENTOFOFOFHEALTHHEALTHHEALTHANDANDANDHUMANHUMANHUMAN ...
NSF的膳食补充剂联邦法规CGMP及食品安全现代法案FSMA 配套法规培训,内容涵盖:21 CFR PART 111,《现行膳食补充剂制造、包装、标识及储存管理规范》及21 CFR PART 117,《人类食品现行良好操作规范和危害分析以及基于风险的预防控制措施》(简称“食品企业预防性控制措施法规”),可帮您了解如何在实际中施行 CGMP的原则要求...
Sustained Compliance MasterControl is fully compliant, which can help you meet FDA 21 CFR Part 111 regulations year after year, while keeping compliance costs down. Integrated Quality Management Products MasterControl is connected, which gives you the ability to monitor the entire quality system and ...
概述:美国《联邦规章典集》(Code of Federal Regulations,CFR)第 21 篇“食品与药品(” Title 21―Food and Drugs)共有 9 卷(Volume)、 3 章(Chapter)、1499 部(Parts)。其中:第 1―8 卷第 1 章第 1―1299 部,为健康与人类服务部食品与药品管理局(Food and Drug Administration,Department of Health ...
(21 CFR Part 11).This document provides guidance to persons who, in fulfillment of a requirement in a statute or another part of FDAs regulations to maintain records or submit information to FDA, have chosen to maintain the records or submit designated information electronically and, as a ...
O T E Introduction 21 CFR Part 11 mandates that electronic records used to support Good Manufacturing Practice (GMP) processes must be main-tained in an environment protected from unauthorized access, use or tampering. One method of providing this environment is by use of a database within a ...
21CFR211中英文对照版(SMART) PART 211 211部分 - CURRENT GOOD MANUFACTURING PRACTICE FOR —制剂药品的CGMP FINISHED PHARMACEUTICALS Subpart A--General Provisions A.总 则 §211.1 - Scope. 211 ∙1范围 §211.3 - Definitions. 211 ∙3定义 Subpart B--Organization and Personnel B.组织与人员 §...