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Number

 

Title

NRC

NUREG 5362

Vol. 1: "Discrete Event Simulation as a Risk Analysis Tool for Remote Afterloading Brachytherapy"

NRC

NUREG 1556

Consolidated Guidance About Materials Licenses: Vol. 9: "Program-Specific Guidance About Medical Use Licenses"

NRC

RIS-2006-19

Availability of Guidance on Radioactive Seed Localization

NRC

HPPOS030

Burial of Patients With Permanent Implants

NRC

HPPOS260

Exemptions from 10 CFR 35.400 for Uses Not Currently Authorized for Iridium-192 Seeds Encased in Nylon Ribbon and Palladium-103 Seeds as Brachytherapy"

NRC

HPPOS273

Evaluation of Comments on NRC Information Notice for Ophthalmic Applicators

NRC

HPPOS287

American Board of Radiology "Certifications"

NRC

HPPOS310

Washington University Medical Center, St. Louis, MO; Authorization to Manipulate Low-Dose Afterloading Brachytherapy

NRC

HPPOS317

Use of Portable Shields for a High Dose Rate Afterloader Facility Washington Hospital Center, Washington, D.C.

NRC

In99002

Guidance to Users on the Implementation of a New Single-Source Dose-Calculation Formalism and Revised Air-Kerma Strength Standard for Iodine-125 Sealed Sources

NRC

In99023

Safety Concerns Related to Repeated Control Unit Failures of the Nucletron Classic Model High-Dose-Rate Remote Afterloading Brachytherapy Devices

NRC

In99027

Malfunction of Source Retraction Mechanism in Cobalt-60 Teletherapy Treatment Units

NRC

In98010

Probable Misadministrations Occurring During Intravascular Brachytherapy with the Novoste Beta-Cath System

NRC

In97064

Potential Problems Associated With Loss of Electrical Power in Certain Teletherapy Units

NRC

In97065

Failures of High-Dose-Rate Remote Afterloading (HDR) Device Source Guide Tubes, Catheters, and Applicators

NRC

In96066

Recent Misadministrations Caused by Incorrect Calibrations of Strontium-90 Eye Applicators

NRC

In96072

Undetected Failures That May Occur During Patient Treatments with Teletherapy Devices

NRC

In95025

Valve Failure During Patient Treatment with Gamma Stereotactic Radiosurgery Unit

NRC

In95039

Brachytherapy Incidents Involving Treatment Planning Errors

NRC

In95050

Safety Defect in Gammamed 12I Bronchial Catheter Clamping Adapters

NRC

In94017

Strontium-90 Eye Applicators: Submission of Quality Management Plan (QMP), Calibration, and Use

NRC

In94039

Identified Problems in Gamma Stereotactic Radiosurgery

NRC

In94065

Potential Error in Manual Brachytherapy Dose Calculations Generated Using a Computerized Treatment Planning System

NRC

In94074

Facility Management Responsibilities for Purchased or Contracted Services for Radiation Therapy Programs

NRC

In93031

Training of Nurses Responsible for the Care of Patients With Brachytherapy Implants

NRC

In92084

Release of Patients Treated With Temporary Implants

NRC

In91002

Brachytherapy Source Management

NRC

In90058

Improper Handling of Ophthalmic Strontium-90 Beta Radiation Applicators

NRC

In90071

Effective Use of Radiation Safety Committees to Exercise Control Over Medical Use Program

NRC

In89060

Maintenance of Teletherepy Units

NRC

In88052

Failure of Intrauterine Tandem of Fletcher Suit Applicator Brachytherapy Devices During Patient Treatment

NRC

In87018

Unauthorized Service on Teletherapy Units by Nonlicensed Maintenance Personnel

NRC

In86084

Rupture of Nominal 40-Millicurie Iodine-125 Brachytherapy Seed Causing Significant Spread of Radioactive Contamination

NRC

In85070

Teletherapy Unit Full Calibration and Qualified Expert Requirements (10 CFR 35.23 and 10 CFR 35.24)

NRC

In84043

Storage and Handling of Ophthalmic Beta Radiation Applicators

NRC

In84062

Therapy Misadministrations To Patients Undergoing Cobalt-60 Teletherapy Treatments

NRC

In82033

Control of Radiation Levels in Unrestricted Areas Adjacent to Brachytherapy Patients

NRC

In80033

Determination of Teletherapy Timer Accuracy

NRC

In80035

Leaking and Dislodged Iodine-125 Implant Seeds

FDA

FDA 79-8079

Handbook of Selected Organ Doses for Projections Common in Pediatric Radiology

FDA

FDA 85-8239

Handbook of Glandular Tissue Doses in Mammography

FDA

FDA 89-8031

Handbook of Selected Tissue Doses for Projections Common in Diagnostic Radiology

FDA

FDA 92-8282

Handbook of Selected Tissue Doses for the Upper Gastrointestinal Fluoroscopic Examination

FDA

FDA 95 - 8289 and 95 - 8288

Handbook of Selected Tissue Doses for Fluoroscopic and Cineangiographic Examination of the Coronary Arteries