Code of Federal Regulations (Last Updated: November 8, 2024) |
Title 10 - Energy |
Chapter I - Nuclear Regulatory Commission |
Part 35 - Medical Use of Byproduct Material |
Subpart B - General Administrative Requirements |
§ 35.20 - ALARA program. |
§ 35.21 - Radiation Safety Officer. |
§ 35.22 - Radiation Safety Committee. |
§ 35.23 - Statements of authority and responsibilities. |
§ 35.24 - Authority and responsibilities for the radiation protection program. |
§ 35.25 - Supervision. |
§ 35.26 - Radiation protection program changes. |
§ 35.27 - Supervision. |
§ 35.29 - Administrative requirements that apply to the provision of mobile nuclear medicine service. |
§ 35.31 - Radiation safety program changes. |
§ 35.32 - Quality management program. |
§ 35.33 - Notifications, reports, and records of misadministrations. |
§ 35.40 - Written directives. |
§ 35.41 - Procedures for administrations requiring a written directive. |
§ 35.49 - Suppliers for sealed sources or devices for medical use. |
§ 35.50 - Training for Radiation Safety Officer and Associate Radiation Safety Officer. |
§ 35.51 - Training for an authorized medical physicist. |
§ 35.55 - Training for an authorized nuclear pharmacist. |
§ 35.57 - Training for experienced Radiation Safety Officer, teletherapy or medical physicist, authorized medical physicist, authorized user, nuclear pharmacist, and authorized nuclear pharmacist. |
§ 35.59 - Recentness of training. |