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Vol. 79Monday,No. 139July 21, 2014Part Nuclear Regulatory Commissiontkelley on DSK3SPTVN1PROD with PROPOSALS210 CFR Parts 30, 32, and 35 Medical Use of Byproduct MaterialMedical Event Definitions,
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10 CFR Part 30 is the code of federal regulations that pertains to rules and regulations related to the licensing of byproduct material.
Any individual or organization that engages in activities involving byproduct material that require a license is required to file 10 CFR Part 30.
To fill out 10 CFR Part 30, you need to provide detailed information about your activities involving byproduct material, including the type of material, quantities involved, and safety measures in place.
The purpose of 10 CFR Part 30 is to ensure the safe and secure use of byproduct material in various applications while minimizing the risk to public health and safety.
Information such as the type and quantity of byproduct material used, license information, safety procedures, and radiation protection measures must be reported on 10 CFR Part 30.
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