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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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Who needs 10 cfr parts 30?
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Organizations or individuals involved in activities related to the possession, use, or transfer of radioactive materials.
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Nuclear facilities, medical institutions, research laboratories, and industrial companies dealing with radioactive substances.
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Anyone seeking to comply with the regulations and requirements set forth by the Nuclear Regulatory Commission (NRC).
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What is 10 cfr parts 30?
10 CFR Part 30 is the code of federal regulations that pertains to rules and regulations related to the licensing of byproduct material.
Who is required to file 10 cfr parts 30?
Any individual or organization that engages in activities involving byproduct material that require a license is required to file 10 CFR Part 30.
How to fill out 10 cfr parts 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.
What is the purpose of 10 cfr parts 30?
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.
What information must be reported on 10 cfr parts 30?
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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