CGA M-5-2008
家用呼吸治疗厂商填充或者分配美国药典(USP)液态氧的指南
Guide for home respiratory care firms filling or distributing liquid oxygen USP
CGA M-5-2008 中，可能用到以下仪器设备
- 标准号
- CGA M-5-2008
- 发布日期
- 2008年
- 实施日期
- 废止日期
- 无
- 中国标准分类号
- G00
- 发布单位
- 美国压缩气体协会
- 引用标准
- United States Pharmacopeia and National Formulary, United States Pharmacopeia, 12601 Twinbrook Pkwy, Rockville, MD 20852. www.usp.org CGA M-2 CGA P-11 Federal Food, Drug, and Cosmetic Act, U.S. Food and Drug Administration, 5600 Fishers Ln., Rockville, M
- 适用范围
- This publication is intended to address operations typical to an HRC firm and is not all inclusive. It is primarily intended for firms engaged in the manufacture and distribution of liquid oxygen USP to patients at their resi- dences. Portions of this publication may apply to those HRC firms that also distribute other compressed medi- cal gases (CMG).This publication includes the minimum regulatory requirements that shall be described in an HRC firm's written standard operating procedures (SOPs) for the firm to receive, fill, test, and distribute liquid oxygen USP and includes the following: - establishment and responsibilities of the quality control unit (QCU); - qualifications of the person(s) performing and supervising the receipt, filling, testing, release, and distribu- tion of liquid oxygen USP; - quality records; - building and facility requirements (including vehicles); - manufacturing equipment design and maintenance; - test equipment; - record and report requirements; - use of computer and other electronic equipment; - receipt and testing of vendor-supplied product into the HRC's storage tank; - receipt and testing of vendor-supplied product into vehicle-mounted vessels (VMVs) or other large cryogenic containers; - receipt and testing of vendor-supplied product into cryogenic home vessels (CHVs); - HRC filling and testing of VMVs and/or large cryogenic containers from an HRC company's storage tank; - HRC filling and testing CHVs; and - labeling requirements. This publication is not applicable to the receipt, testing, release, and distribution of high pressure oxygen filled by HRC firms. Firms engaged in filling high pressure medical gas cylinders (either gas-to-gas or liquid-to-gas) should refer to CGA M-2, General Guide for the Manufacturer of Medical Gases Classified as Drugs. This publication is typically not applicable to non-HRC firms unless those firms are engaged in activities similar to those of HRC firms. Non-HRC firms engaged in oxygen USP liquid-to-liquid filling for home care use should also refer to CGA M-2 for additional guidance and potential additional regulatory requirements.