Application for license, amendment, or renewal.

CFR · 2024-01-01 · US · Title 10

(a) An application must be signed by the applicant's or licensee's management. (b) An application for a license for medical use of byproduct material as described in §§ 35.100, 35.200, 35.300, 35.400, 35.500, 35.600, and 35.1000 must be made by— (1) Filing an original NRC Form 313, “Application for Material License,” that includes the facility diagram, equipment, and training and experience qualifications of the Radiation Safety Officer, Associate Radiation Safety Officer(s), authorized user(s), authorized medical physicist(s), ophthalmic physicist(s), and authorized nuclear pharmacist(s); and (2) Submitting procedures required by §§ 35.610, 35.642, 35.643, and 35.645, as applicable. (c) A request for a license amendment or renewal must be made by— (1) Submitting an original of either— (i) NRC Form 313, “Application for Material License”; or (ii) A letter containing all information required by NRC Form 313; and (2) Submitting procedures required by §§ 35.610, 35.642, 35.643, and 35.645, as applicable. (d) In addition to the requirements in paragraphs (b) and (c) of this section, an application for a license or amendment for medical use of byproduct material as described in § 35.1000 must also include: (1) Any additional aspects of the medical use of the material that are applicable to radiation safety that are not addressed in, or differ from, subparts A through C, L, and M of this part; (2) Identification of and commitment to follow the applicable radiation safety program re

official document · source cfr-2024 · id 10:§ 35.12