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 ...
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 ...
PART 211 211部分 - CURRENT GOOD MANUFACTURING PRACTICE FOR —制剂药品的CGMP FINISHED PHARMACEUTICALS Subpart A--General Provisions § - Scope. 211∙1范围 § - Definitions. 211∙3定义 Subpart B--Organization and Personnel § - Responsibilities of quality control unit. 211∙22质量控制部门的职...
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 §...
Part 211 - CURRENT GOOD MANUFACTURING PRACTICE FOR FINISHED PHARMACEUTICALS Subpart A - General Provisions Sec. 21 1 .1 Scope. 21 1 .3 Definitions. Subpart B - Organization and Personnel 21 1 .22 Responsibilities of quality control unit. 21 1 .25 Personnel qualifications. 21 1 .28 ...
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 §...
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 §211.22 - Responsibilities of ...
物料系统(CGMP21CFR211分录E和H) 72 说明:文件中绿色突出显示的内容是FDA2008年12月8日修订执行的新要求. 六大体系通用的法规分录B&J SubpartB--OrganizationandPersonnelB.组织与人员 Sec.211.22Responsibilitiesofqualitycontrolunit. 211∙22质量控制部门的职责 (a)Thereshallbeaqualitycontrolunitthatshallhavethere...
Meng_8x6创作的外语有声书作品21CFR211 cGMP for FP,目前已更新11个声音,收听最新音频章节SUBPART I laboratory controls。
in parts 211 through 226 of this chapter in the manufacture, processing, packing, or holding of a drug shall render such drug to be adulterated under section 501(a)(2)(B) of the act and such drug, as well as the person who is responsible for the failure to comply, shall be sub-...