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Current as of January 02, 2025 | Updated by Findlaw Staff
(a) A licensee shall maintain a record of dosage determinations required by § 35.63 for 3 years.
(b) The record must contain—
(1) The radiopharmaceutical;
(2) The patient's or human research subject's name, or identification number if one has been assigned;
(3) The prescribed dosage, the determined dosage, or a notation that the total activity is less than 1.1 MBq (30 μCi);
(4) The date and time of the dosage determination; and
(5) The name of the individual who determined the dosage.
Cite this article: FindLaw.com - Code of Federal Regulations Title 10. Energy § 10.35.2063 Records of dosages of unsealed byproduct material for medical use - last updated January 02, 2025 | https://codes.findlaw.com/cfr/title-10-energy/cfr-sect-10-35-2063/
FindLaw Codes may not reflect the most recent version of the law in your jurisdiction. Please verify the status of the code you are researching with the state legislature before relying on it for your legal needs.
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