To solicit comments from the public and stakeholders on the NRC's evaluation of the training and experience (T&E) requirements for a physician to become an authorized user for medical uses under Subpart E, “Unsealed Byproduct Material—Written Directiv

To solicit comments from the public and stakeholders on the NRC's evaluation of the training and experience (T&E) requirements for a physician to become an authorized user for medical uses under Subpart E, “Unsealed Byproduct Material—Written Directive Required,” of Title 10 of the Code of Federal Regulations (10 CFR) Part 35, “Medical Use of Byproduct Material.” Notice soliciting comments was published in the Federal Register on October 29, 2018 (83 FR 54380).