Nevada Administrative Code
Chapter 459 - Hazardous Materials
RADIATION CONTROL
Licensing of Radioactive Material
Section 459.296 - Specific licenses: Manufacture or distribution of radioactive material for in vitro clinical or laboratory testing

1. The applicant satisfies the general requirements specified in NAC 459.238.

2. The radioactive material is to be prepared for distribution in prepackaged units of:

3. Each prepackaged unit bears a durable, clearly visible label:

4. The following statement, or a substantially similar statement which contains the information called for in the following statement, appears on a label affixed to each prepackaged unit or appears in leaflet or brochure which accompanies the package:

This radioactive material may be received, acquired, possessed and used only by physicians, clinical laboratories or hospitals and only for in vitro clinical or laboratory tests not involving internal or external administration of the material, or the radiation therefrom, to human beings or animals. Its receipt, acquisition, possession, use and transfer are subject to the regulations and a general license of the Nuclear Regulatory Commission or of a state with which the Commission has entered into an agreement for the exercise of regulatory authority.

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Name of Manufacturer

5. The label affixed to the unit, or the leaflet or brochure which accompanies the package, contains adequate information regarding the precautions to be observed in handling and storing such radioactive material. In the case of the mock iodine-125 reference or calibration source, the information accompanying the source must also contain directions to the licensee regarding the waste disposal requirements of NAC 459.3355 and 459.359 to 459.3615, inclusive.