Chapter 10 Flashcards
An EfD limiting system has been incorporated into what title of Federal Regulations
Title 10, Part 20
Title 10, Part 20 is a document prepared and distributed by the:
US Office of the Federal Register
What is the basis of the EfD Limiting System
Concept of radiation exposure and of the assiocated risk of radiation-induced malignancy
What reports revised the EfD limiting system
NCRP Report 116
ICRP Report 60
What is in Title 10 of the Code of Federal Regulations besides dose limits
Rules and regulations of the NRC and fundamental radiation protection standards governing occupational radiation exposure
Reasons medical imaging professionals must be familiar with previous, exisiting, and new guidelines for radiation safety
Share the responsibility for patient safety
Subject to radiation exposure in the performance of their duties
How many organizations are responsible for evaluating the relationship between radiation EqD and induced biologic effects
4
What are the 4 radiation protection standards organizations?
International Commission on Radiological Protection (ICRP)
National Council on Radiation Protection and Measurements (NCRP)
United Nations Scientific Committee on the Effects of Atomic Radiation (UNSCEAR)
National Academy of Sciences/National Research Council Committee on the Biological Effects of Ionizing Radiation (NAS/NRC-BEIR)
What organization evaluates information on biological effects of radiation and provides radiation protection guidance through general recommendations on occupational and public dose limits
International Commission on Radiological Protection
Organization that reviews regulations formulated by the ICRP and decides ways to include those recommendations in US radiation protection criteria
NCRP
Organization that evaluates human and environmental ionizing radiation exposure and derives radiation risk assessments from epidemiologic data and research conclusions; provides information to organizations such as the ICRP for evaluation
UNSCEAR
Organization that reviews studies of biological effects of ionizing radiation and risk assessment and provides the information to organizations such as the ICRP for evaluation
NAS/NRC-BEIR
Objectives of the NCRP (Public Law 88-376)
1.Collect, analyze, develop and desseminate information about radiaiton measurements concerned with radiation protection
- Provide a means by which organizations may cooperate for utilization of their combined resources
- Develop basic concepts about radiation quantities and protection
- Cooperate with ICRP and other national/international organizations
US regulatory agencies
Nuclear Regulatory Commission (NRC)
Agreement states
Enivronmental Protection Agency (EPA)
US Food and Drug Administration (FDA)
Occupational Safety and Health Administration (OSHA)
Organization that oversees the nuclear energy industry, enforces radiation protection standards, publishes its rules and regulations to Title 10, and enters into agreements with state govementments that permit the state to license and regulate the use of radioisotopes and certain other material within the state
NRC
Enforce radiation protection regulations through their respective health departments
Agreeable states
Facilitiates the development and enforcement of regulations pertaining to the control of radiation in the environment
EPA
Conducts an ongoing product radiation control program, regulating the design and manufacture of electronic products, including x-ray equipment
FDA
Functions as a monitoring agency in places of employment, predominately in industry
OSHA
Facilities providing imaging services must have an effective and detailed:
Radiation safety program
Steps for implementing an effective radiation safety progarm
Begins with administration personnel
Executives must provide the resources for creating and maintaing the program
Functions of Radiation Safety Committee
Provides guidance for the program
Facilitates ongoing operation of program
Selects a qualified person to serve as a radiation safety officer
Who is responsible for the oversee of the program’s daily operations and provides for a formal review of the program each year
RSO
RSO is normally a:
Medical physicist
Health physicist
Radiologist
Qualified through experience and training
RSO has been designated by a health care facility and approved by:
NRC and the state
Develops radiation safety program that follows internationally accepted guidelines
RSO
Who grants the RSO the authority necessary to implement and enforce policies of the radiation safety program
Management of the facility
Other responsibilities of RSO:
Review and maintain monitoring records for all personnel
Be available to provide counseling
Necessary training and experience for an RSO are described in what sections of the Code of Federal Regulations:
10 CFR 35.50
10 CFR 35.900
What are the three training pathways for an RSO
Certification by one of the professional boards approved by the NRC
Didactic and work experience as described in the regulations
Identification as an authorized user, authorized medical physicist, or authorized nuclear physicist on the license, with experience in the types of uses for which the individual has RSO responsibilities
10 CFR 35.24 requires that the licensee provide the RSO:
Sufficient authority
Organizational freedom
Management prerogative to perform specific duties
A radiation safety officer in a health care facility must have sufficient authority, organizational freedom, and management prerogative to
Identify radiation safety problems
Initiate, recommend, or provide corrective action
Stop unsafe operations involving by-product material
Verify implementation of corrective actions
The authority, duties, and responsibilites of the RSO must be established in:
Writing
Why does the NRC require the name of the RSO on the facilities radioactive materials license
To ensure that licensee management has always identified a responsible, qualified person who can directly interact with the NRC during inspections and also concerning any inquiries about the facility’s safety program
Usually the RSO is a ________ employee
Full-time
Purpose of Radiaition Control for Health and Safety Act of 1968
To protect the public from the hazards of unnessary radiation exposure resulting from electronic products such as microwave ovens and picture tube colors TVs
Radiation Control for Health and Safety 1968 permitted the estatblishment of:
The Center for Devices and Radiological Health (CDRH)
CDRH falls under the jurisdiction of the:
FDA
CDRH is responsible for:
Conducting an ongoing electronic product radiation control program
What law is strictly an equipment performance standards
Law 90-602
Code of Standards for Diagnostic X-ray Equipment went into effect on:
Aug 1, 1974
ALARA concept was put forth in what year and by who
1954 by the NCRP
ALARA is also known as
Optimization
The continuation of good radiation protection programs and practicies which traditionally have been effective in keeping the average and individual exposures for monitoring workers below the limit
ALARA