Code of Maine Rules
10 - DEPARTMENT OF HEALTH AND HUMAN SERVICES
144 - DEPARTMENT OF HEALTH AND HUMAN SERVICES - GENERAL
Chapter 220 - Rules Relating to Radiation Protection
Part C - LICENSING OF RADIOACTIVE MATERIAL
SPECIFIC LICENSES
Section 144-220-C-7 - Filing application for specific licenses
Current through 2024-38, September 18, 2024
A. Applications for specific license shall be filed on a form prescribed by the Agency.
B. The Agency may at any time after the filing of the original application, and before the expiration of the license, require further statements in order to enable the Agency to determine whether the license should be modified or revoked.
C. Each application shall be signed by the applicant or licensee or a person duly authorized to act for and on their behalf.
D. An application for a license filed pursuant to this rule will be considered also as an application for a license authorizing other activities for which licenses are required, provided that the application specifies the additional activities for which the license is requested and complies with the appropriate regulations.
E. All sections of the application must be completed, clearly and concisely, with the applicable required information and submitted with the applicable fee, if required.
F. Applications and documents submitted to the Agency may be made available for public inspection except that the Agency may withhold any document or part thereof from public inspection if disclosure of its content is not required in the public interest and would adversely affect the interest of a person concerned.
G. Except as provided in paragraphs C.7.H, I, and J, an application for a specific license to use byproduct material in the form of a sealed source or in a device that contains the sealed source must either:
H. For sources or devices manufactured before October 23, 2012 that are not registered with the NRC under 10 CFR 32.210 or with an Agreement State, and for which the applicant is unable to provide all categories of information specified in 10 CFR 32.210(c), the applicant must provide:
I. For sealed sources and devices allowed to be distributed without registration of safety information in accordance with C.7.G of this rule, the applicant may supply only the manufacturer, model number, and radionuclide and quantity.
J. If it is not feasible to identify each sealed source and device individually, the applicant may propose constraints on the number and type of sealed sources and devices to be used and the conditions under which they will be used, in lieu of identifying each sealed source and device.
K. An application from a medical facility, educational institution, or Federal facility to produce positron emission tomography (PET) radioactive drugs for noncommercial transfer to licensees in its consortium authorized for medical use under Part G or equivalent Agreement State requirements shall include:
L. Emergency Planning