美国《联邦规章典集》(CFR)第21篇“食品与药品”总目.pdf,美国《联邦规章典集》(CFR )第 21 篇 “食品与药品”总目 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
FDA 医疗器械法规 CFR-2021-title21-vol8-part860.pdf,Food and Drug Administration, HHS § 860.3 PART 860—MEDICAL DEVICE sification of devices intended for CLASSIFICATION PROCEDURES human use. (b) This part prescribes the criteria Subpart A—General and pr
美国医疗器械法规CFR-2021-title21-vol8-part812.docx,Food and Drug Administration, HHS § 812.1 agency determines that such notifica- tion may cause unnecessary and harm- ful anxiety in individuals and that ini- tial consultation between individuals and th
FDA 医疗器械法规 CFR-2021-title21-vol8-part820.pdf,Pt. 820 21 CFR Ch. I (4–1–21 Edition) reasonably should be known to the ap- Subpart E—Purchasing Controls plicant, medical device reports made under part 803 of this chapter, any data 820.50 Purchasin
美国《联邦规章典集》（CFR）第21篇“食品与药品”总目概述：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 ...
美国《联邦规章典集》（CFR）第21篇“食品与药品”总目概述：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（V olume）、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...
FDA 医疗器械法规 CFR-2021-title21-vol8-part807.pdf,Food and Drug Administration, HHS Pt. 807 device. Records required to be main- Subpart B—Procedures for Device tained under paragraph (b) of this sec- Establishments tion must be transferred to the new
美国联邦政府法规29CFR1910“职业安全与健康标准”..doc,Title 29: Labor PART 1910—OCCUPATIONAL SAFETY AND HEALTH STANDARDS Contents Subpart A—General § 1910.1 Purpose and scope. § 1910.2 Definitions. § 1910.3 Petitions for the issuance, amendment, or r
美国FDA《联邦规章典集》(CFR)第21篇目录中文版-推荐下载
[Code of Federal Regulations][Title 21, Volume 2][Revised as of April 1, 2013][CITE: 21CFR110.10]TITLE 21--FOOD AND DRUGS CHAPTER I--FOOD AND DRUG ADMINISTRATION DEPARTMENT OF HEALTH AND HUMAN SERVICES SUBCHAPTER B--FOOD FOR HUMAN CONSUMPTION PART 110 -- CURRENT GOOD MANUFACTURING PRACTICE...