内容提示: 21 CFR PARTS 210 & 211; Revised as of April 1st 1997 Page 1 of 24 RECORDS_SIGS GMP.doc PART 210-CURRENT GOOD MANUFACTURING PRACTICE IN MANUFACTURING, PROCESSING, PACKING, OR HOLDING OF DRUGS; GENERAL ...3 §210.1 Status of current good manufacturing practice regulations......
PART210CURRENTGOODMANUFACTURINGPRACTICEIN MANUFACTURING,PROCESSING,PACKING,OR HOLDINGOFDRUGS;GENERAL Sec.210.1Statusofcurrentgoodmanufacturingpracticeregulations. (a)Theregulationssetforthinthispartandinparts211through226ofthischaptercontaintheminimumcurrentgoodmanufacturingpracticeformethodstobeusedin,andthefacilitiesorco...
(a) The regulations in this part and in Parts 211 through 226 of this chapter as 210210 部分部分——人用及兽用药品的生产、加人用及兽用药品的生产、加工、包装或贮存的工、包装或贮存的 cGMPcGMP 210.1 cGMP 法规的地位 210.2 cGMP 法规的适用性 210.3 定义 210.1 cGMP210.1 cGMP 法规的地位法规的...
21CFR210中英文对照版(SMART).pdf,Part 210 - CURRENT GOOD MANUFACTURING 210 部分— 人用及兽用药 品的生产 、加工、包装或贮存 的 PRACTICE IN MANUFACTURING, PROCESSING, CGMP PACKING, OR HOLDING OF DRUGS; GENERAL 210.1 Status of current good manufacturing prac
PART 211 - CURRENT GOOD MANUFACTURING PRACTICE FOR FINISHED PHARMACEUTICALS 211部分 —制剂药品的CGMP Subpart A--General Provisions §211.1 - Scope. §211.3 - Definitions. A.总则 211∙1范围 211∙3定义 Subpart B--Organization and Personnel §211.22 - Responsibilities of quality control unit. §...
21CFR211中文对照版(SMART).pdf,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--Orga
cGMP21CFR210211中英对照 21 Code of Federal Regulations Parts 210 and 211 Part 210 - CURRENT GOOD MANUFACTURING PRACTICE IN MANUFACTURING, PROCESSING, PACKING, OR HOLDING OF DRUGS; GENERAL PART 211 ? - CURRENT GOOD MANUFACTURING PRACTICE FOR FINISHED PHARMACEUTICALS 210部分—人用及兽用药品的生产、...
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 §...
1、.:.;21 Code of Federal Regulations Parts210 and 211Part 210 - CURRENT GOOD MANUFACTURING PRACTICE IN MANUFACTURING, PROCESSING, PACKING, OR HOLDING OF DRUGS; GENERAL HYPERLINK /scripts/cdrh/cfdocs/cfcfr/CFRSearch.cfm?CFRPart=211 PART 211 - CURRENT GOOD MANUFACTURING PRACTICE FOR FI 2、NI...