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、...
21 CFR Parts 210 and 211 Regulations Document Control Subpart F, Section 211.100 – There shall be written procedures for production and process control, assuring that drug products have the intended identity, strength, quality, and purity. Written procedures, including any changes, shall be ...
内容提示: 21 CFR Parts 210 and 211 - Current Good Manufacturing Practice In Manufacturing, Processing, Packing or Holding of Drugs; General and Current Good Manufacturing Practice For Finished Pharmaceuticals Revisions as of 2 May 2006 Part 210 - CURRENT GOOD MANUFACTURING PRACTICE IN MANUFACTURING, ...
21-CFR-210&211-cGMP中英对照版currentgoodmanufacturingpracticeforfinishedpharmaceuticals210部分人用及兽用药品的生产加工包装或贮存的cgmp概述211部分制剂药品的cgmppart210currentgoodmanufacturingpracticeinmanufacturingprocessingpackingorholdingofdrugs 21 Code of Federal Regulations Parts 210 and 211 Part 210 - ...
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、加工、包装或贮存的 CGMP(...
GENERAL PART 211 - CURRENT GOOD MANUFACTURING PRACTICE FOR FINISHED PHARMACEUTICALS 210 部分—人用及兽用药品的生产、 加工、 包装或贮存的 CGMP(概述) 211 部分—制剂药品的 CGMP 21 Code of Federal Regulations Parts 210 and 211 Part 210 - CURRENT GOOD MANUFACTURING PRACTICE IN MANUFACTURING, PROCESSING...
《美国联邦法规》(Code of FederalRegulations, CFR)是将发表在“联邦公报(Federal Register, FR)”的一般性和永久性法规集合成册的法规典籍。CFR的法规涵盖各方面主题,其中第21篇“食品与药品”就是美国食品药品监督管理局(Food and DrugAdministration, FDA)管理食品和药品的主要法规依据。所谓知己知彼,百战不殆。做...
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......
21CFR Part 210&211 中英文对照版_2020.4 PART210 CURRENT GOOD MANUFACTURING PRACTICE IN MANUFACTURING,PROCESSING,PACKING, OR HOLDING OF DRUGS;GENERAL 210部分 人用及兽用药品的生产、包装或储存的现行药品生产质量管理规范 （通则）第1页共72页