Quality Management Program

Technical Report · Tue Oct 01 00:00:00 EDT 1991

DOI:https://doi.org/10.2172/6164103· OSTI ID:6164103

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.

• Research Organization: US Nuclear Regulatory Commission (NRC), Washington, DC (United States). Office of Nuclear Regulatory Research
• Sponsoring Organization: USNRC; Nuclear Regulatory Commission, Washington, DC (United States)
• OSTI ID: 6164103
• Report Number(s): REG/G-8.33; ON: TI92002342
• Country of Publication: United States
• Language: English

Related Subjects

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