Preparation, Transfer for Commercial Distribution, and Use of Byproduct Material for Medical Use
other · Nuclear Regulatory Commission · Published 1995-01-04 · Effective 1995-01-01 · 60 FR 322
Document
Document number
95-00124
Federal Register citation
60 FR 322
CFR reference
10 CFR 32
Type
Rule
Action
Final rule; clarification.
Category
other
Sub-agency
Nuclear Regulatory Commission
Publication date
1995-01-04
Effective date
1995-01-01
Abstract
The Nuclear Regulatory Commission (NRC) is amending regulatory text and the response to a public comment contained in a final rule published in the Federal Register on Friday, December 2, 1994, entitled ``Preparation, Transfer for Commercial Distribution, and Use of Byproduct Material for Medical Use.'' This action is necessary following reconsideration by the NRC regarding the requirements for the information to be included on labels for radioactive drugs to be transferred for commercial distribution. The effect of this action is to reduce regulatory burden and uncertainty for licensees that manufacture and distribute radiopharmaceuticals that contain byproduct material for medical use.