§111.23-UnderthissubpartC,whatrecordsmustyoumakeandkeep? SubpartD--EquipmentandUtensils §111.25-WhataretherequirementsunderthissubpartDforwrittenprocedures? §111.27-Whatrequirementsapplytotheequipmentandutensilsthatyouuse? §111.30-Whatrequirementsapplytoautomated,mechanical,orelectronicequipment? §111.35-Under...
CFR 11-111.12-2014 联邦选举. 第111部分:合规程序(52 U.S.C. 30109, 30107(a)). 214(C)). 第A子部分:执行. 第111.12节:传票和出庭出示证明的传票;口供(52 U.S.C. 30107(a)(3), (4)). Federal elections. Part111:Compliance procedure (52 U.S.C. 30109, 30107(a)). SubpartA:Enforcemen...
PART 111第111 CURRENT GOOD MANUFACTURING PRACTICE IN MANUFACTURING, PACKAGING, LABELING, OR HOLDING OPERATIONS FOR DIETARY SUPPLEMENTS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 Subpart A--General Provisions子部分-一般规定 Sec.秒。111.1 Who is subject to this part? 111.1谁是受这部分?
第111.31节:这个子部分取代了第A子部分违反了52 U.S.C. 30104(a)的报告要求吗? Federal elections. Part111:Compliance procedure (52 U.S.C. 30109, 30107(a)). SubpartB:Administrative fines. Section111.31:Does this Subpartreplace SubpartA of this part for violations of the reporting requirements...
CFR=CodeofFederalRegulations美国联邦法规21章第11款电子记录和电子签名http://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfcfr/cfrsearch.cfm?cfrpart=11 概述 1997年8月20日颁布实施的法规适用于包括现有体系内所有FDA监管的工作中的电子记录电子签名和电子记录的准则：可信的和可靠的电子签名=手写...
(111.12(b)项) Subpart C – Physical Plant and Grounds ? You must have written procedures for cleaning the physical plant and for pest control. (111.16) ? If water is a component of the dietary supplement, you must review water records to make certain that the water complies with ...
(111.12(b)项) Subpart C – Physical Plant and Grounds ? You must have written procedures for cleaning the physical plant and for pest control. (111.16) ? If water is a component of the dietary supplement, you must review water records to make certain that the water complies with ...
(111.8) •您必须有员工培训的文档,包括培训日期和培训类型。 (111.14) •您必须确定是谁负责质量控制以及他们的资质。 (111.12(b)项) Subpart C – Physical Plant and Grounds • You must have written procedures for cleaning the physical plant and for pest control. ...
内容提示: TITLE 21--FOOD AND DRUGS CHAPTER I--FOOD AND DRUG ADMINISTRATION DEPARTMENT OF HEALTH AND HUMAN SERVICES SUBCHAPTER B--FOOD FOR HUMAN CONSUMPTION PART 111--CURRENT GOOD MANUFACTURING PRACTICE IN MANUFACTURING, PACKAGING, LABELING, OR HOLDING OPERATIONS FOR DIETARY SUPPLEMENTS Subpart A--...
21 CFR Part 111 - Section 111.570(b)2(ii) of subpart O Written records of product complaints must be kept and must include the (A) the name and description of the dietary supplement; (B) the batch, lot, or control number of the dietary supplement, if available; (C) the date the ...