Standard roster

Individual standards in this cluster

EPA MB-26-03 and ASTM E2967 form the citation set; ARE Labs translates them into residual efficacy study design, neutralization checks, wear conditioning, QA records, and report outputs.

EPA

EPA MB-26-03

EPA MB-26-03 anchors the neutralization check that shows residual active chemistry is stopped before survivor enumeration.

Aligned
ASTM

ASTM E2967

ASTM E2967 is officially withdrawn with no replacement.

Aligned

Purpose & when to use

Residual antimicrobial efficacy studies ask whether treated surfaces, coatings, residues, textiles, or articles keep measurable activity after drying, use, abrasion, aging, or repeat microbial challenge. This Standards cluster helps teams decide how EPA MB-26-03 neutralization controls and ASTM E2967 legacy Wiperator context should inform a residual study without overstating either source:

  1. EPA residual sanitizer programs use MB-26-03 when neutralization and recovery controls must show active chemistry does not bias viable counts.
  2. ASTM E2967 may support legacy Wiperator towelette comparisons when a client protocol still cites the withdrawn method.
  3. EPA antimicrobial-product claim work uses this cluster when wear, drying, aging, and re-challenge timing must be documented together.
  4. Material programs use ASTM or EPA context when treated and untreated surfaces need comparable recovery, controls, and durability trends.

Use this cluster when the core question is persistent antimicrobial activity after use-relevant stress. ARE Labs scopes the surface, organism, active chemistry, wear condition, neutralizer, recovery endpoint, and report package before protocol approval.

Applicable to

Built around residual surface claims

The cluster applies when a residual sanitizer, coating, treated article, fabric, or device-facing surface must be challenged after drying, handling, abrasion, aging, or repeat contact.

Standards in this group

What each citation controls

This page is a cluster, not a claim that one citation fully governs every residual wear program. EPA MB-26-03 is an official neutralization SOP used to support recovery validity in quantitative hard-surface antimicrobial work. ASTM E2967 is a withdrawn Wiperator towelette method retained only when a legacy protocol or comparison frame specifically cites it.

EPA
Aligned

EPA MB-26-03

Neutralization of Microbicidal Activity using the Quantitative Method for Evaluating Bactericidal and Mycobactericidal Activity of Microbicides Used on Hard, Non-Porous Surfaces

EPA MB-26-03 anchors the neutralization check that shows residual active chemistry is stopped before survivor enumeration. ARE Labs uses it to design neutralizer suitability, recovery controls, treated and untreated comparisons, and report language for hard, non-porous residual antimicrobial studies where the SOP applies.

EPA official method page verified 2026-05-17; page lists Method ID MB-26-03 and date 2020-11-24.

ASTM
Aligned

ASTM E2967

Standard Test Method for Assessing the Ability of Pre-wetted Towelettes to Remove and Transfer Bacterial Contamination on Hard, Non-Porous Environmental Surfaces Using the Wiperator

ASTM E2967 is officially withdrawn with no replacement. ARE Labs treats it as legacy context for Wiperator-based towelette removal or transfer comparisons when a client program cites it; residual wear protocols should document why this withdrawn method remains relevant before use.

ASTM official store page verified 2026-05-17; page lists ASTM E2967-15 withdrawn in 2024 with no replacement.

Aligned by protocol, not certified as a blanket claim

ARE Labs treats this cluster as standards-aligned residual antimicrobial support. Neither EPA MB-26-03 nor ASTM E2967 is marked as formally accredited in the current allowlist, and ISO 17025 is described only as the quality-system posture where applicable.

  • EPA MB-26-03AlignedNeutralization SOP applied where protocol fit is confirmed.
  • ASTM E2967AlignedWithdrawn Wiperator method used only for legacy citations.
  • ISO 17025AlignedQuality-system framing, not citation-specific accreditation.
Operational chain

How ARE Labs turns the standards into a study

The citations do not define every residual wear scenario by themselves. ARE Labs converts EPA and ASTM context into a protocol that fits the product, material, organism, active chemistry, wear sequence, recovery endpoint, and documentation objective.

01
Scope

Define the residual claim

We map the EPA or ASTM citation to the treated surface, organism, contact time, drying interval, wear condition, and comparison groups.

Protocol matrix
02
Controls

Prove neutralization and recovery

EPA MB-26-03 framing drives neutralizer suitability, recovery controls, active-quench checks, and survivor enumeration before efficacy is interpreted.

Control record
03
Conditioning

Apply wear or aging stress

EPA claim support and ASTM legacy comparisons document abrasion media, wipe sequence, aging interval, environmental conditions, and re-challenge timing.

Conditioning log
04
Adaptation

Handle method-fit limits

When ASTM E2967 is cited despite withdrawn status, ARE Labs records why the legacy Wiperator context fits the product question.

Rationale note
05
Reporting

Connect survivors to durability

Reports tie EPA recovery controls, ASTM limitations, viable counts, log or percent reduction, deviations, and wear-stage trends to the study objective.

Reviewed report

Data quality, QA/QC & documentation

Residual antimicrobial results are only useful when the control record explains how survivors were recovered and counted. ARE Labs ties EPA and ASTM citation context to sample identity, wear settings, neutralization checks, environmental records, raw counts, calculations, deviations, and final QA review.

Connect sample to citation

EPA and ASTM records link sample ID, surface preparation, application method, drying time, wear condition, and organism challenge to the selected study frame.

Verify recovery before interpretation

EPA MB-26-03 neutralization evidence shows residual active chemistry was controlled before survivor counts, log reduction, or percent reduction are reported.

Preserve wear-stage details

ASTM legacy comparisons and EPA claim support retain abrasion cycles, wiping load, aging interval, chamber conditions, and re-challenge timing.

Retain raw and reduced counts

EPA and ASTM study files include plate counts, dilution factors, calculations, control acceptance notes, deviations, and durability trend summaries.

Separate alignment from approval

ISO 17025 review language distinguishes ARE Labs quality controls from EPA registration decisions, ASTM certification, or withdrawn-method endorsement.

Why ARE Labs

ARE Labs connects technical topics to practical study design, method selection, controlled aerosol work, and reportable evidence without turning technical pages into sales pages.

Reviewed byJamie Balarashti (25 yrs - cascade & inhalation methods) - Weston Schaper (7 yrs - real-time sizing & nanoparticle work)
QualityDocumented study records
900+Studies Performed
17+Years in operation
300+Clients supported

Common questions

These questions cover how residual antimicrobial programs use EPA MB-26-03, ASTM E2967, and fit-for-purpose protocols without overclaiming what each citation controls. The answers identify the scoping decisions ARE Labs resolves before protocol drafting, sample conditioning, microbial recovery, interpretation, QA review, final reporting, and regulator-facing evidence planning begins.

Q. Is EPA MB-26-03 a residual wear method?

A. No. EPA MB-26-03 is a neutralization SOP. ARE Labs uses it to support recovery validity in residual antimicrobial studies when the protocol needs that control evidence.

Q. Can ASTM E2967 still be used?

A. Only with care. ASTM lists E2967 as withdrawn with no replacement, so ARE Labs uses it only when a legacy protocol or comparison frame specifically requires it.

Q. What does aligned mean here?

A. Aligned means ARE Labs follows the cited method or guidance by protocol where it fits. It does not mean EPA approval, ASTM certification, or citation-specific accreditation.

Q. What if my product does not fit either citation?

A. ARE Labs can develop a fit-for-purpose residual protocol that documents the selected wear condition, recovery controls, deviations, and limits of interpretation.

Q. What data does the report include?

A. Reports can include sample maps, wear conditions, neutralization checks, raw counts, reductions, control recovery, deviations, trend summaries, and a reviewed technical interpretation.