A FIPS 140-3 validation belongs to one defined cryptographic module: its name, version, boundary, tested operational environments, services, security ratings, and caveats. The vendor prepares the module and evidence, an accredited Cryptographic and Security Testing laboratory tests it, and reviews the submitted report and decides whether to validate it. Publication is not the end of the lifecycle. Product owners and buyers must keep checking the live record, Security Policy, sunset date, guidance and algorithm transitions, vulnerabilities, dependencies, and implementation changes before reusing the claim.
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Section 1
Separate the standard timeline from the module lifecycle
FIPS 140-3 was issued on March 22, 2019 and superseded FIPS 140-2. began accepting FIPS 140-3 submissions on September 22, 2020. The standard's implementation schedule records program transition milestones; it does not set a recurring deadline for every commercial product.
changes its technical interpretations and management procedures over time. The official pages checked on 15 October 2026 identify an August 19, 2026 Implementation Guidance edition and an April 9, 2026 Management Manual edition. A submission must use the applicable requirements and guidance at the relevant submission stage, so record the edition used for each decision and recheck the official pages before a new or updated submission.
A module project runs on its own evidence and review sequence. Timing depends on when the vendor freezes scope, finishes evidence, engages a laboratory, closes findings, and enters review. FIPS 140-3 says the review schedule varies with coordination among the vendor, laboratory, and CMVP. Neither an listing nor a state promises a validation date.
A separate procurement transition ended in September 2026: the cited FAQ set September 21, 2026 as the last day FIPS 140-2 validations remained on the Active list, with only FIPS 140-3 validations remaining Active from September 22, 2026. This status transition does not convert a FIPS 140-2 certificate into FIPS 140-3 or validate a changed product.
March 22, 2019 | FIPS 140-3 issued | Standard publication, not a module certificate.
September 22, 2020 | began accepting FIPS 140-3 submissions | Start of the program's FIPS 140-3 submission activity.
April 9, 2026 | Management Manual edition listed by | Record the edition applicable to the submission.
August 19, 2026 | Implementation Guidance edition listed by on 15 October 2026 | Recheck the announcements before relying on a technical interpretation.
September 21, 2026 | Last day FIPS 140-2 validations remain on the Active list under current policy | Recheck the live certificate before procurement or continued claim use.
September 22, 2026 | Only FIPS 140-3 validations remain on the Active list | permits continued use of FIPS 140-2 modules for existing systems only; the transition does not establish FIPS 140-3 validation.
Use the module project plan for design freeze, laboratory testing, finding closure, submission, review, and release decisions.
Record which version of implementation guidance supports each submission decision because the guidance can change.
Treat transition dates as specific to the affected algorithm, evidence path, or submission scenario rather than as blanket module deadlines.
Records the September 22, 2020 submission start and permits continued use of Historical FIPS 140-2 modules for existing systems only after the September 2026 transition.
The April 9, 2026 management source for process states, participant responsibilities, validation status, and submission scenarios.
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Section 2
Who does what before validation
The vendor defines the implementation under test: its boundary, version, interfaces, roles, services, operational environments, security ratings, approved security functions, Security Policy, and supporting evidence. The vendor contracts with an accredited Cryptographic and Security Testing laboratory. The independently evaluates the module, performs required testing, prepares the report, and submits the package. , jointly managed by NIST and the Canadian Centre for Cyber Security, reviews the submission and makes the validation decision.
algorithm testing supports the package but does not replace module validation. A CAVP certificate identifies a tested algorithm implementation and operational environment. The certificate detail connects the defined module to its Security Policy, caveats, status, and algorithm references.
The buyer or system owner does not repeat laboratory testing. The buyer verifies the public entry and reads the Security Policy to decide whether the deployed module, version, environment, services, and caveats meet the system's requirements. If a validated module is embedded in a larger product, CMVP does not assure that the product invokes it correctly.
Vendor: freeze the module identity and boundary, prepare required documentation, resolve test findings, and approve the exact public claim.
: independently test the module, assess vendor evidence, document results, submit the package, and work with the vendor and to resolve review comments.
: review the report and clarifications, decide whether to validate, and publish or update the public validation record.
Buyer or system owner: verify that the deployed module, version, environment, services, certificate status, Security Policy, and caveats match the intended use.
Defines the CMVP, vendor use of independent accredited laboratories, laboratory testing role, and submission of test reports for CMVP review and validation.
Explains the user verification role and the limit on claims for products that contain embedded validated modules.
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Section 3
Lifecycle workflow: owner, evidence, and exit decision
Use one versioned record through the lifecycle rather than recreating scope for each team. The record should let an engineer, laboratory, reviewer, release owner, and buyer identify the same module and distinguish planned scope, tested claims, submitted claims, and completed validation.
Public process labels are not certificates. The Implementation Under Test list is voluntary and covers modules undergoing laboratory testing whose reports have not been submitted; says it does not know whether or when those reports will arrive. The list tracks specified submission types after CMVP receives the report and shows states such as Pending Review, Cost Recovery, Review, Comment Resolution, Finalization, or Hold. Only the published validation entry establishes completed validation.
Step 1, Scope and design freeze. Owner: Vendor. Evidence: boundary diagram, module/version manifest, interfaces, roles, services, target levels, operational environments. Exit question: Is the implementation under test unambiguous?
Step 2, Evidence preparation. Owner: Vendor with laboratory input. Evidence: Security Policy, requirement mapping, algorithm and entropy evidence, self-test results, physical and lifecycle evidence. Exit question: Is the package ready for independent testing?
Step 3, Conformance testing. Owner: Accredited . Evidence: test results, reviewed vendor evidence, findings, final test report. Exit question: Does the tested module satisfy the claimed requirements?
Step 4, Submission and review. Owner: , vendor, and CMVP. Evidence: submitted package, cost-recovery record where applicable, comments, responses, corrected evidence, and review state. Exit question: Has CMVP completed review and accepted this exact module and claim?
Step 5, Publication and release. Owner: and vendor. Evidence: public module record, certificate details, non-proprietary Security Policy, caveats, release claim. Exit question: Does the shipped configuration match the public record?
Step 6, Maintenance and reassessment. Owner: Vendor, laboratory when needed, and product owner. Evidence: change-impact record, status check, Common Vulnerabilities and Exposures (CVE) analysis, updated evidence or revalidation submission. Exit question: Can the existing validation still be relied on?
Do not call a module validated while its submission is planned, on the list, in laboratory testing, on the list, or under review.
Keep the public Security Policy and customer wording aligned with the module record and any caveats.
Escalate an unresolved version, boundary, operational-environment, algorithm, or dependent-module mismatch before release or procurement.
Preserve dated evidence of the public-status check because status can change after the original validation.
Sections 1.7.8 and 4.1 explain the IUT and Modules in Process lists, public review states, participant duties, and the testing-and-validation sequence.
Recommended next step
Track FIPS 140-3 validation and maintenance
Keep module scope, laboratory evidence, CMVP review responses, public claims, status checks, and post-validation changes connected in one accountable workflow.
Validation is not a permanent whole-product approval. Assess changes to hardware, software, firmware, excluded components, the boundary, services, algorithm implementations, operating systems, processors, hypervisors, entropy sources, and bound or embedded modules against the validated configuration and current rules before shipping the old claim.
Section 7.1 of the current Management Manual defines twelve submission scenarios. An updated version may use revalidation rather than full validation depending on the extent and type of change; if it does not meet a revalidation scenario, it must undergo full validation. The vendor reviews every FIPS 140-3 requirement affected by the change, while the independently evaluates the impact and performs the required testing.
guidance requires CVE assessment during and after validation. A module need not be free of every CVE, but the vendor must determine applicability and security relevance and document mitigation where needed. For a post-validation security-relevant CVE or maintenance fix, work with a on the applicable CVE, Update, or Full Submission path; do not patch the module and keep using the old claim without that assessment.
Run change impact before shipping a changed configuration with an existing FIPS 140-3 claim.
Track the status and used functionality of any bound or embedded validated module; the relying module can inherit status from that dependency.
Maintain a CVE register that distinguishes applicable, non-applicable, security-relevant, mitigated, and unresolved entries with rationale.
Use the applicable submission scenario instead of inventing a certificate-maintenance label or assuming a documentation-only update is enough. Administrative wording with no FIPS impact may fit a Vendor Update, but documentation that changes assessed assertions can require laboratory reassessment even when code is unchanged.
Section 7.1 defines full-validation and revalidation scenarios and assigns change-impact and testing responsibilities to the vendor and CST laboratory.
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Section 5
Status and procurement claims
Before procurement or customer assurance relies on a certificate, check the live record rather than a supplier slide, an old Security Policy copy, or a algorithm result. Record the module name, version, certificate number, status, sunset date, tested environments, Security Policy, caveats, approved services, and the product configuration that invokes the module.
Active is the default status for a newly validated module. Current policy generally places FIPS 140-3 validations on the Active list for five years; an is valid for two years unless converted through the applicable follow-up process. The certificate's actual sunset date controls the record, and programmatic transitions can move a validation to sooner.
means the record is no longer Active because of age, current guidance, or a programmatic transition; it does not mean the module never passed validation. FIPS 140-3 warns that the Historical list is for reference and should not be used for procurement decisions, although the Management Manual allows an agency to make a documented risk decision about continued use. means the validation is no longer valid and may not be cited to demonstrate FIPS 140 conformity.
Say 'uses FIPS 140-3 validated module [name/version/certificate]' when that accurately describes the product; do not label the entire product validated by implication.
Say 'validation in progress' only when that process status is accurate, and never present it as completed validation.
Do not describe algorithm certification, vendor affirmation, laboratory readiness, or a passed internal test as validation.
Recheck the public record at contract renewal, major release, environment change, algorithm transition, dependency status change, security-relevant vulnerability, and before the recorded sunset date.
Current official management source for process states, participant responsibilities, validation status, and full-validation or revalidation submission scenarios.
The April 9, 2026 management source for process states, participant responsibilities, validation status, and submission scenarios.
Sections 1.7.8 and 4.1 explain the IUT and Modules in Process lists, public review states, participant duties, and the testing-and-validation sequence.
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Section 7.1 defines full-validation and revalidation scenarios and assigns change-impact and testing responsibilities to the vendor and CST laboratory.
Sections 4.7 and 7.1.2.1 explain Historical and Revoked treatment and the two-year Interim Validation period.
Primary source for program roles, implementation chronology, variable review timing, CMVP conformance, and procurement status cautions.
Supports the 22 March 2019 issue date, supersession of FIPS 140-2, relative implementation schedule, and variable CMVP review timing.
Defines the CMVP, vendor use of independent accredited laboratories, laboratory testing role, and submission of test reports for CMVP review and validation.
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Grounds the laboratory-testing and CMVP-review sequence and the limit that modules validated under CMVP are considered conforming.
Supports the procurement use of the validated modules list and the explicit warning against using Historical-list entries for procurement decisions.
"review and validation"
More quoted passages
"The review process schedule varies"
"A test report for modules demonstrating compliance will be submitted to the CMVP for review and validation"
"CMVP Historical list should not be used for procurement decisions"
Current program guidance for submissions, algorithm validation evidence, approved services, operational environments, CVEs, dependent modules, transitions, and change handling.
Official technical guidance for FIPS 140-3 implementations and CMVP interpretations; verify the edition applicable to the submission.
Distinguishes CAVP algorithm validation evidence from CMVP cryptographic module validation and supplies current submission interpretations.
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Grounds post-validation CVE handling, revalidation references, operational-environment dependencies, and Historical-status inheritance for bound or embedded modules.
"subject to change by NIST and CCCS"
More quoted passages
"CMVP is not requiring that the module and associated equipment be free from CVEs"
Official explanations of the buyer's verification role, product-versus-module scope, Active, Historical, Revoked, and sunset status, and the September 21-22, 2026 FIPS 140-2 Active-list transition.
Explains the user verification role and the limit on claims for products that contain embedded validated modules.
Defines Active, Historical, Revoked, and sunset status and explains what each means for use of a validation record.
Current overview for FIPS 140-3 program milestones and general Active and Interim validation periods.
Records the September 22, 2020 submission start and permits continued use of Historical FIPS 140-2 modules for existing systems only after the September 2026 transition.
States the current general five-year Active period for FIPS 140-3 validations and the two-year period for Interim Validations.