10 CFR 35.2063, Records of Dosages of Unsealed Byproduct Material for Medical Use
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Records of dosages of unsealed byproduct material for medical use
a
(a) A licensee shall maintain a record of dosage determinations required by § 35.63 for 3 years.
b
(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.
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