IAEA GSR Part 3 — Radiation Protection and Safety of Radiation Sources: International Basic Safety Standards (2014)
1. Source documents
- Official PDF retained locally — IAEA and joint sponsoring organisations, 2014; retrieved 16 September 2026.
- Extracted text
- Provenance and SHA-256 metadata
2. Authority and jurisdiction
- IAEA General Safety Requirements jointly sponsored by relevant international organisations.
- Establishes requirements for states and organisations within its international standards framework; it is not directly binding Queensland legislation.
- Influences Australian codes including RPS C-1 and RPS C-5. Local legal force requires national or jurisdictional implementation.
3. Key takeaways
- GSR means General Safety Requirements: GSR Part 3 sets international requirements for radiation protection and source safety across planned, emergency and existing exposure situations, with governmental, regulatory and responsible-person duties.
- Planned exposure requirements distinguish occupational, public and medical exposure and apply the protection principles differently to each.
- Patient medical exposure is controlled by justification and optimisation, with defined professional responsibilities, calibration, dosimetry, QA and investigation—not by applying occupational/public dose limits to the prescribed treatment.
- Requires a graded approach, management for protection and safety, competence, safety assessment, prevention and mitigation, and records.
- Provides the international requirements layer underneath ARPANSA codes and IAEA SSG-46, not a direct approval or licence for THHS.
4. Summary
4.1. 1 — Introduction
- Defines background, objective, scope, structure and the relationship to the IAEA safety principles.
4.2. 2 — General requirements for protection and safety
- Sets responsibilities of government, regulatory bodies and principal parties.
- Requires justification, optimisation, dose limitation where applicable, graded control, management systems, safety assessment, prevention and emergency preparedness.
4.3. 3 — Planned exposure situations
- Requirement 9 and paras 3.13–3.15 assign primary protection and safety responsibility to registrants and licensees, including organisational measures and documented delegation. This is an international role framework, not a Queensland possession licence.
4.3.1. Government and regulatory framework
- Requires authorisation, review, inspection, enforcement and supporting infrastructure proportionate to radiation risk.
4.3.2. Occupational exposure
- Covers area classification, engineered and administrative controls, local rules, worker monitoring, dose assessment, health surveillance and records.
- Requirement 24 places local rules and workplace monitoring within a radiation protection programme. Paragraph 3.94(e) calls for an RPO where appropriate under regulatory criteria; para 3.96 places workplace monitoring under an RPO or qualified expert.
- Paragraph 3.110 requires worker instruction, training, periodic retraining and records. The RPO role is not the Queensland statutory RSO certificate.
4.3.3. Public and environmental exposure
- Covers source-related public exposure, discharges, monitoring, assessment and environmental protection.
4.3.4. Medical exposure
- Allocates responsibilities among the radiological medical practitioner, medical radiation technologist and medical physicist.
- Requires justification, optimisation, appropriate equipment, calibration, patient dosimetry, QA, special consideration of pregnancy and breast-feeding, and investigation of unintended or accidental medical exposure.
- Biomedical research exposure requires ethics approval (paras 3.152 and 3.161); significant unintended or accidental exposure is reported under para 3.181, subject to national implementation.
4.4. 4 — Emergency exposure situations
- Establishes preparedness, response, worker and public protection, reference levels, transition and review requirements.
4.5. 5 — Existing exposure situations
- Addresses identified existing exposures, remediation and radon or other source-specific control using reference levels and optimisation.
4.6. Schedules
- Schedule I
- Exemption and clearance.
- Schedule II
- Categorisation of sealed sources.
- Schedule III
- Dose limits for planned exposure situations.
- Schedule IV
- Criteria for emergency preparedness and response.
5. Important definitions, roles, limits and records
- Requirement
- A statement necessary to meet the IAEA safety standards framework; domestic enforceability still depends on implementation.
- Dose constraint and reference level
- Prospective optimisation tools; neither is simply interchangeable with a dose limit.
- Medical physicist
- Health professional with specialist education and training in the concepts and techniques of applying physics in medicine, competent to practise independently in relevant subfields.
- Limits
- Schedule III addresses worker and public exposure; patient medical exposure is excluded from dose limitation and instead controlled by justification and optimisation.
- Records
- Authorisations, occupational dose, calibration, dosimetry, QA, patient exposure, incidents and emergency arrangements as applicable.
6. Practical relationship to the THHS RSPP
- International requirements source for the RSPP's differentiated treatment of patient, worker and public exposure.
- Supports role clarity, safety assessment, training, calibration/dosimetry, QA, pregnancy management and unintended-exposure investigation.
- Use RPS C-1/C-5 and Queensland instruments to state the Australian and binding local implementation.