Regulatory Text
42 C.F.R. § 11.40 — Who must submit clinical trial results information?
§ 11.40 Who must submit clinical trial results information? The responsible party for an applicable clinical trial specified in § 11.42 must submit clinical trial results information for that clinical trial.
Source: ecfr.gov · govinfo.gov — public domain
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Root-LD Entity Data
◈ Machine-Readable Provenance Record
Root-LD v1.0 · boisestandard.org
Federation ID
BS-CFR42-SEC-990107
Entity Class
REGULATION / FEDERAL-CFR-SECTION
Domain Signature
boisestandard.org
Citation
42 C.F.R. § 11.40
Corpus
CFR — Code of Federal Regulations
Status
✓ ACTIVE
Source
PRIMARY-SOURCE
Source Verified
✓ TRUE
Content Hash
88416d3dbee829ce...
Semantic Edges
Pending — corpus passes queued
The regulatory text of 42 C.F.R. § 11.40 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.
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Title 42 — Public Health
42 C.F.R. § 2a.142 C.F.R. § 2a.242 C.F.R. § 2a.342 C.F.R. § 2a.442 C.F.R. § 2a.542 C.F.R. § 2a.642 C.F.R. § 2a.742 C.F.R. § 2a.842 C.F.R. § 2.142 C.F.R. § 2.242 C.F.R. § 2.342 C.F.R. § 2.442 C.F.R. § 2.1142 C.F.R. § 2.1242 C.F.R. § 2.1342 C.F.R. § 2.1442 C.F.R. § 2.1542 C.F.R. § 2.1642 C.F.R. § 2.1742 C.F.R. § 2.1842 C.F.R. § 2.1942 C.F.R. § 2.2042 C.F.R. § 2.2142 C.F.R. § 2.2242 C.F.R. § 2.2342 C.F.R. § 2.3142 C.F.R. § 2.3242 C.F.R. § 2.3342 C.F.R. § 2.3442 C.F.R. § 2.35
42 C.F.R. — public domain
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