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Nonclinical Testing Terminology
Health and Human Services Department; Food and Drug Administration: final rule. Dated 43 days ago, it serves as a historical benchmark. Score 45/100. As of 2026-11-03, from Federal Register API (Office of the Federal Register).
Data as of · Compiled by Zalwin from Federal Register API (Office of the Federal Register)
Free preview: all 10 published fields of this record are shown below. Locked: 62 related FederalRegisterCompliancePulse records and the 5-column CSV export.
| Field | Value |
|---|---|
| Agency | Health and Human Services Department; Food and Drug Administration |
| Type | Final rule |
| Action | Direct final rule. |
| Published | 2026-09-22 |
| Effective | 2027-02-04 |
| Comments close | 2026-12-07 |
| Significant | No |
| CFR parts | 21 CFR 312, 21 CFR 314, 21 CFR 315, 21 CFR 361, 21 CFR 601 |
| Summary | The Food and Drug Administration (FDA, Agency, or we) is issuing a direct final rule that substitutes references to "animal" tests or studies with "nonclinical" tests or studies, adds a definition of the terms "nonclinical test" and "nonclinical study," and makes other comparable or conforming amendments in certain safety and reporting sections of its regulations. The direct final rule also substitutes "nonclinical" for "preclinical" and "in vitro" for consistency in terminology. The Agency is issuing these amendments directly as a final rule because we believe they are noncontroversial change |
| Document number | 2026-19350 |
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- Source agency: Federal Register API (Office of the Federal Register)
- Record date: 2026-09-22
- Data refreshed: 2026-11-03
- Refunds on request within 14 days
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LIVE PUBLIC DATA Source: Federal Register API (Office of the Federal Register) · Last refreshed: Tue, 03 Nov 2026 19:10:06 GMT
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Peer benchmark and outreach value: Health and Human Services Department; Food and Drug Administration and 63 food-and-drug-administration peers
- food-and-drug-administration FederalRegisterCompliancePulse records like this one: 63
- Timing: Low: older than 30 days
- Estimated pipeline if you contact every food-and-drug-administration peer: $12,600 (peers × rate × deal size; an estimate from your assumptions, not a forecast)
45 / 100 Action Urgency Score
- Upcoming deadline.
- Final rule.
What is the FederalRegisterCompliancePulse record for Health and Human Services Department; Food and Drug Administration?
Health and Human Services Department; Food and Drug Administration published a final rule on 2026-09-22, effective 2027-02-04, comments due 2026-12-07: Nonclinical Testing Terminology.
How does Health and Human Services Department; Food and Drug Administration compare to other FederalRegisterCompliancePulse records?
It is 43 days old, still within a typical 45-day follow-up window.
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Data from the Federal Register API; the published Federal Register document is authoritative. Informational only, not legal advice.