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U.S. Nuclear Regulatory Commission. Office of Nuclear Regulatory Research.

  • Disposition of recommendations of the National Research Council in the report Revitalizing nuclear safety researchDisposition of recommendations of the National Research Council in the report Revitalizing nuclear safety research
  • Draft regulatory guide DG-0003Draft regulatory guide DG-0003
  • Draft regulatory guide DG-1107Draft regulatory guide DG-1107
  • Draft regulatory guide DG-1129Draft regulatory guide DG-1129
  • Draft regulatory guide DG-7004Draft regulatory guide DG-7004
  • General site suitability criteria for nuclear power stationsGeneral site suitability criteria for nuclear power stations
  • Guidance for implementation of 10 CFR 72.48, changes, tests, and experimentsGuidance for implementation of 10 CFR 72.48, changes, tests, and experiments
  • Guidance for the preparation of supplemental environmental reports in support of an application to renew a nuclear power station operating licenseGuidance for the preparation of supplemental environmental reports in support of an application to renew a nuclear power station operating license
  • Guide for the preparation of application for commercial nuclear pharmacy licensesGuide for the preparation of application for commercial nuclear pharmacy licenses
  • Guide for the preparation of applications for licenses to authorize distribution of various items to commercial nuclear pharmacies and medical use licensesGuide for the preparation of applications for licenses to authorize distribution of various items to commercial nuclear pharmacies and medical use licenses
  • Preparation of petitions for rulemaking under 10 CFR 2.802 and preparation and submission of proposals for regulatory guidance documentsPreparation of petitions for rulemaking under 10 CFR 2.802 and preparation and submission of proposals for regulatory guidance documents
  • Proposed supplement to regulatory guide 10.8, revision 2, "Guide for the preparation of applications for medical use programs"Proposed supplement to regulatory guide 10.8, revision 2, "Guide for the preparation of applications for medical use programs"