Regulatory Text
10 C.F.R. § 35.2063 — Records of dosages of unsealed byproduct material for medical use.
§ 35.2063 Records of dosages of unsealed byproduct material for medical use. (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.
Source: ecfr.gov · govinfo.gov — public domain
Official Source ↗
Root-LD Entity Data
◈ Machine-Readable Provenance Record
Root-LD v1.0 · boisestandard.org
Federation ID
BS-CFR10-SEC-47510F
Entity Class
REGULATION / FEDERAL-CFR-SECTION
Domain Signature
boisestandard.org
Citation
10 C.F.R. § 35.2063
Corpus
CFR — Code of Federal Regulations
Status
✓ ACTIVE
Source
PRIMARY-SOURCE
Source Verified
✓ TRUE
Content Hash
34b59eb5c93ae5c9...
Semantic Edges
Pending — corpus passes queued
The regulatory text of 10 C.F.R. § 35.2063 is reproduced from the official Code of Federal Regulations as published by the Office of the Federal Register and the National Archives and Records Administration.
Navigate Corpus — Title 10 C.F.R.
Title 10 — Energy
10 C.F.R. § 1.110 C.F.R. § 1.310 C.F.R. § 1.510 C.F.R. § 1.1110 C.F.R. § 1.1210 C.F.R. § 1.1310 C.F.R. § 1.1510 C.F.R. § 1.1810 C.F.R. § 1.1910 C.F.R. § 1.2310 C.F.R. § 1.2410 C.F.R. § 1.2510 C.F.R. § 1.2610 C.F.R. § 1.2710 C.F.R. § 1.2810 C.F.R. § 1.2910 C.F.R. § 1.3110 C.F.R. § 1.3210 C.F.R. § 1.3310 C.F.R. § 1.3410 C.F.R. § 1.3510 C.F.R. § 1.3610 C.F.R. § 1.3710 C.F.R. § 1.3810 C.F.R. § 1.3910 C.F.R. § 1.40.1.4110 C.F.R. § 1.4210 C.F.R. § 1.4310 C.F.R. § 1.4410 C.F.R. § 1.45
10 C.F.R. — public domain
← All Legislation