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Title: Quality Management Program

Abstract

According to {section} 35.32, Quality Management Program,'' of 10 CFR Part 35, Medical Use of Byproduct Material,'' applicants or licensees, as applicable, are required to establish a quality management (QM) program. This regulatory guide provides guidance to licensees and applicants for developing policies and procedures for the QM program. This guide does not restrict or limit the licensee from using other guidance that may be equally useful in developing a QM program, e.g., information available from the Joint Commission on Accreditation of Healthcare Organizations or the American College of Radiology. Any information collection activities mentioned in this regulatory guide are contained as requirements in 10 CFR Part 35, which provides the regulatory basis for this guide. This information collection requirements in 10 CFR Part 35 have been cleared under OMB Clearance No. 3150-0010.

Publication Date:
Research Org.:
Nuclear Regulatory Commission, Washington, DC (United States). Office of Nuclear Regulatory Research
Sponsoring Org.:
USNRC; Nuclear Regulatory Commission, Washington, DC (United States)
OSTI Identifier:
6164103
Report Number(s):
REG/G-8.33
ON: TI92002342
Resource Type:
Technical Report
Country of Publication:
United States
Language:
English
Subject:
62 RADIOLOGY AND NUCLEAR MEDICINE; 29 ENERGY PLANNING, POLICY AND ECONOMY; 99 GENERAL AND MISCELLANEOUS//MATHEMATICS, COMPUTING, AND INFORMATION SCIENCE; BY-PRODUCTS; REGULATORY GUIDES; NUCLEAR MEDICINE; ADMINISTRATIVE PROCEDURES; QUALITY CONTROL; RADIOPHARMACEUTICALS; RADIOTHERAPY; BIOMEDICAL RADIOGRAPHY; LICENSING; MANAGEMENT; MEDICAL ESTABLISHMENTS; MEDICAL PERSONNEL; QUALITY ASSURANCE; RADIATION DOSES; REGULATIONS; CONTROL; DIAGNOSTIC TECHNIQUES; DOCUMENT TYPES; DOSES; DRUGS; LABELLED COMPOUNDS; MEDICINE; PERSONNEL; RADIOLOGY; THERAPY; 550600* - Medicine; 293000 - Energy Planning & Policy- Policy, Legislation, & Regulation; 990100 - Management

Citation Formats

. Quality Management Program. United States: N. p., 1991. Web. doi:10.2172/6164103.
. Quality Management Program. United States. https://doi.org/10.2172/6164103
. Tue . "Quality Management Program". United States. https://doi.org/10.2172/6164103. https://www.osti.gov/servlets/purl/6164103.
@article{osti_6164103,
title = {Quality Management Program},
author = {},
abstractNote = {According to {section} 35.32, Quality Management Program,'' of 10 CFR Part 35, Medical Use of Byproduct Material,'' applicants or licensees, as applicable, are required to establish a quality management (QM) program. This regulatory guide provides guidance to licensees and applicants for developing policies and procedures for the QM program. This guide does not restrict or limit the licensee from using other guidance that may be equally useful in developing a QM program, e.g., information available from the Joint Commission on Accreditation of Healthcare Organizations or the American College of Radiology. Any information collection activities mentioned in this regulatory guide are contained as requirements in 10 CFR Part 35, which provides the regulatory basis for this guide. This information collection requirements in 10 CFR Part 35 have been cleared under OMB Clearance No. 3150-0010.},
doi = {10.2172/6164103},
url = {https://www.osti.gov/biblio/6164103}, journal = {},
number = ,
volume = ,
place = {United States},
year = {1991},
month = {10}
}