USP General Chapter <825> Impact on Nuclear Medicine Technology Practice

被引:7
作者
Hinkle, George H. [1 ]
机构
[1] Ohio State Univ, Environm Hlth & Safety, Radiat Safety Off, 1314 Kinnear Rd, Columbus, OH 43212 USA
关键词
USP < 825 >; radiopharmaceutical compounding; sterile radiopharmaceutical; USP standards;
D O I
10.2967/jnmt.120.243378
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
U.S. Pharmacopeia (USP) general chapter <825>, "Radiopharmaceuticals: Preparation, Compounding, Dispensing, and Repackaging," is a new standard proposed to provide minimum requirements for the preparation, compounding, dispensing, and repackaging of sterile and nonsterile radiopharmaceuticals. This new standard represents endeavors on the part of the USP to respond to appeals by nuclear medicine professionals to move beyond a minimal supplement to USP <797>. and provide policies specific to radiopharmaceuticals. USP <825> provides nuclear pharmacies and nuclear medicine departments in hospitals and clinics with the benchmarks to assess current practice activities and integrate needed changes to meet regulatory and accreditation audit reviews. This continuing education article focuses on components of USP <825> specific to the nuclear medicine technologist for a better understanding of obligations when preparing sterile radiopharmaceuticals for clinical use.
引用
收藏
页码:106 / 113
页数:8
相关论文
共 3 条
  • [1] SNMMI-TS Scope Practice Task Force, 2017, J NUCL MED TECHNOL, V45, P53
  • [2] USP-NF, 2019, RAD PREP COMP DISP R
  • [3] USP-NF, 2016, PHARM COMP STER PREP