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Compliance

Compliance, at the scale modern operators actually need.

GFSI, GxP, MDR, ESPR, IATF, REACH, CPR — 80+ frameworks across 20 industries, driven by one platform. Map a control once, cite it everywhere it counts.

  • Compliance that compiles itself — one platform, every framework
  • 80+ industry frameworks across 20 regulated sectors
  • 47 country regulators with format-native submissions
  • Currency tracked: QMSR (Feb 2026), PPWR (Aug 2026), CPR 2024 active
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Compliance
Live
GFSI readiness · 5 schemesComposite 92%

  • BRCGS

    Issue 9 · Food

    Active

  • SQF

    Ed. 9 · Food Safety

    Active

  • FSSC 22000

    v6 · Manufacturing

    In renewal

  • IFS

    Food v8

    Audit in 14d

  • GLOBALG.A.P.

    IFA v6 · Crops

    Submission

All 5 schemes mapped to your platform · single source of evidence

The problem

Compliance shouldn't run on a parallel system.

Most operators run compliance like a separate department — folders per framework, spreadsheets per audit, and the same evidence rekeyed five times. The result: a tax on every market you enter, paid in headcount and missed renewals. At 80+ frameworks across 20 industries, the rekey tax becomes unrunnable.

Parallel paperwork

One folder per framework. Same evidence, rekeyed 4 times — and now versions drift.

Audit-quarter scramble

Audit notice lands, your team disappears for three weeks assembling artefacts. Real work stops.

Framework duplication tax

Add a market, add a framework, add headcount. Compliance scales linearly with regulators — until it breaks.

Renewal blindness

Certifications lapse in inboxes nobody monitors. Expiry surprises cost shipments and market access.

Map once, satisfy many

One control. Every framework that asks for it.

These are three illustrative examples — food safety, pharmaceutical, and medical devices. Across the platform we map 80+ frameworks onto one audit trail, with every cell auto-populated from the same source events.

Compliance controls mapped across BRCGS, SQF, FSSC 22000, IFS, FDA frameworks. Each row shows how one control satisfies citations in all five frameworks simultaneously.
Your controlBRCGSSQFFSSC 22000IFSFDA
CCP monitoring records§ 3.7.1§ 2.4.4§ 7.2.1§ 4.20§ 117.150
Allergen control procedure§ 5.3§ 11.7§ 7.4.2§ 4.20.1§ 117.135
Supplier approval list§ 3.5.1§ 2.3.3§ 7.1.5§ 4.4.1§ 117.405
Pest control log§ 4.14.1§ 11.2.13§ 8.1.4§ 4.13§ 117.35(c)
Internal audit programme§ 3.4.1§ 2.5.4§ 9.2§ 5.11§ 117.165
Capabilities

Six capabilities, one platform.

Built across the deepest regulatory surface in the platform space — 80+ frameworks across 20 industries, every one driven by the same six core capabilities.

Multi-framework mapping

Single evidence item, multiple framework citations. Map a control once, cite it everywhere BRCGS, SQF, FSSC 22000, IFS, and GLOBALG.A.P. need it.

Automated monitoring

Compliance posture updates as your operation runs. CCP excursions, missed PRPs, expired certs surface immediately — not at audit time.

Regulator submission generation

FDA 21 CFR, EU 178/2002, ANVISA, FSSAI, NAFDAC — regulator-specific report formats assembled from the same audit trail.

Audit scheduling & history

Calendar of upcoming audits, certificate expiries, and renewal windows. Auditor portal access with scoped read-only views.

Document control & versioning

Every policy, procedure, and SOP versioned, signed, and approval-tracked. Diff view between revisions. Auditors see the chain.

Evidence library

Auto-assembled per control. One source event, many citations — the library is generated, not curated by hand.

Framework portfolio

The full portfolio, day one.

Seven framework families covering food safety, pharma, medical devices, sustainable products, automotive, chemicals, and construction — each with the most-deployed standards mapped on day one. The long tail (PrimusGFS, CanadaGAP, JFS-C, GRMS, ASIAGAP, and more) lands via custom mapping on Premium and Enterprise.

5 most-deployed GFSI-recognised food safety schemes

Issue 9

BRCGS

Food · Packaging · Storage & Distribution · Agents & Brokers

Edition 9

SQF

Primary production through retail · Food Safety + Quality codes

v6

FSSC 22000

Food manufacturing · Packaging · Animal feed · Catering

Food v8

IFS

Food · Broker · Logistics · Household & Personal Care

IFA v6

GLOBALG.A.P.

Primary production · Aquaculture · Produce · Flowers & Ornamentals

Regulators we speak

Submissions that match the regulator's format.

Every regulator wants their own format, their own field names, their own export rules. Traceage ships region-specific submission generators across 47 countries — same evidence, regulator-shaped output. Format-native, not just labels: we track regulator format changes as they ship.

GCC

4 countries · Gulf Cooperation Council

  • BahrainNHRA · MOH
  • QatarMOPH
  • Saudi ArabiaSFDA
  • UAEESMA · MOHAP · Dubai Municipality

Europe

10 countries + EU-wide bodies

  • DenmarkDVFA
  • EU-wideEFSA · ECHA · EMA · DG SANTE
  • FranceDGAL · ANSM
  • GermanyBVL · BfArM
  • IrelandHPRA · FSAI
  • ItalyMinistero della Salute
  • MaltaMCCAA · MMA
  • NetherlandsNVWA
  • SpainAESAN
  • SwitzerlandSwissmedic · FSVO
  • United KingdomFSA · MHRA · DEFRA

Africa

18 countries · food, pharma, agriculture

  • AlgeriaANPP · ALGERAC
  • BotswanaBORA · BOBS
  • EgyptNFSA · EDA
  • EthiopiaEFDA
  • GhanaFDA Ghana · GSA
  • GuineaANSS
  • Ivory CoastAIRP · CODINORM
  • KenyaKEBS · PPB
  • MauritiusMSB · Pharmacy Board
  • MoroccoONSSA
  • NigeriaNAFDAC · SON
  • RwandaRwanda FDA
  • SenegalDAPSA · ARP
  • South AfricaDALRRD · SAHPRA
  • TanzaniaTBS · TMDA
  • UgandaUNBS · NDA
  • ZambiaZABS · ZAMRA
  • ZimbabweMCAZ · SAZ

Americas

5 countries · Americas regulators

  • ArgentinaANMAT · SENASA
  • BrazilANVISA · MAPA
  • CanadaCFIA · Health Canada
  • MexicoCOFEPRIS · SENASICA
  • United StatesFDA · USDA · EPA

Asia-Pacific

10 countries · APAC regulators

  • AustraliaFSANZ · TGA
  • ChinaSAMR
  • IndiaFSSAI · CDSCO
  • IndonesiaBPOM · BSN
  • JapanMHLW · CAA
  • MalaysiaBKKM · NPRA
  • New ZealandMPI · Medsafe
  • SingaporeSFA · HSA
  • South KoreaMFDS
  • TaiwanTFDA

Markets not on the prebuilt list. Burkina Faso, Cameroon, DRC, and other emerging markets can be added via custom regulator mapping (available on Premium and Enterprise). We're actively engaging with regulators in these markets to capture their submission formats, and we monitor regulatory framework changes across all listed jurisdictions.

KYC / KYB hub

Know Your Customer. Know Your Business.

The central hub for identity, beneficial ownership, sanctions, and adverse media checks. Continuous, not point-in-time — re-screened on schedule and on regulator list updates.

Supplier · ACME-7748

Acme Foods Inc · São Paulo, Brazil

CNPJ 12.345.678/0001-90 · screened 2026-03-14 09:42 UTC

Verified

Sanctions & screening matrix

  • OFAC (US Treasury)

    SDN List, Sectoral, Non-SDN

    Clear

  • EU Consolidated List

    Council Regulation 269/2014 et seq.

    Clear

  • UK HMT

    OFSI Consolidated

    Clear

  • UN Security Council

    Consolidated Sanctions List

    Clear

  • PEP screening

    Politically Exposed Persons (global)

    Clear

  • Adverse media

    Negative news, 30+ jurisdictions

    Clear

Next re-screen: 2026-06-14 · cadence 90d · auto-rescreened on every regulator list update in between.

What KYC / KYB unlocks

Beneficial-ownership and sanctions screening are no longer optional — every modern due-diligence framework treats them as table stakes. We shipped it on day one.

  • EU Regulation 2023/1115 — EUDR (deforestation due diligence)
  • EU CSDDD — Corporate Sustainability Due Diligence Directive
  • German Supply Chain Act (LkSG)
  • UK Modern Slavery Act 2015 · Australian Modern Slavery Act
  • Canada Bill S-211 — Fighting Against Forced Labour
  • EU 6AMLD — Sixth Anti-Money Laundering Directive

Third-party verification providers integrated — Sumsub, Onfido, Trulioo, Persona. Per-check fees pass through transparently.

Sample submission

FDA 21 CFR § 117.150 evidence pack.

A real submission output, assembled from the same audit trail. The regulator gets a pack shaped to their schema; you get one source of truth. Every record links back to its underlying event with a verifiable signature.

  • Auto-assembled from raw events — no manual collation
  • Regulator-shaped output as JSON, signed PDF on demand
  • Every cell links back to source event with hash
  • Re-issuable on demand — no re-keying
submission-fda-117-150.jsonSigned
{
  "submission_id": "sub-2026-03-14-fda-44819",
  "regulation": "21 CFR § 117.150",
  "filer": {
    "facility": "FCE-19847",
    "registration": "FDA-FCE-19847-2026"
  },
  "scope": {
    "framework": "FDA Preventive Controls",
    "period": "2026-Q1",
    "records_count": 4128
  },
  "evidence": [
    {
      "control": "CCP-04 thermal",
      "events": 2114,
      "deviations": 0,
      "source_ref": "evt://2026-q1/ccp-04",
      "hash": "0x8a2c…d3f1"
    },
    {
      "control": "Allergen segregation",
      "events": 1872,
      "deviations": 2,
      "source_ref": "evt://2026-q1/allergen",
      "hash": "0x4b1d…e7c9"
    }
  ],
  "signature": "0x9f3a…c2b8",
  "issued_at": "2026-04-01T08:00:00Z"
}
By industry

Built for every regulated sector.

Frameworks shift by industry, but the engine doesn't. 20 industries, 80+ frameworks, all mapped onto one platform — from food and pharma to construction and aerospace.

Food & beverage

GFSI’s deepest deployment surface — every certification built on HACCP. Same evidence powers FSMA 204 traceability and 21 CFR § 117 Preventive Controls in the US.

  • HACCP
  • BRCGS
  • SQF
  • FSSC 22000
  • IFS Food
  • 21 CFR § 117

Pharmaceutical

GxP from manufacturing through supply-chain serialization. DSCSA (US, fully enforceable since May 2025) + EU FMD across all 27 EU members; ICH harmonisation built in.

  • GMP
  • ICH Q7-Q10
  • DSCSA
  • EU FMD
  • FDA 21 CFR Part 11
  • EMA

Cosmetics & personal care

EU 1223 product safety + FDA MoCRA reporting + ISO 22716 GMP + EU CLP for ingredient classification.

  • EU 1223/2009
  • FDA MoCRA
  • ISO 22716
  • EU CLP

Medical devices

FDA QMSR replaced 21 CFR 820 in Feb 2026, harmonising US with ISO 13485. MDSAP audits 6 markets (US, EU, Canada, Brazil, Australia, Japan) in one cycle.

  • FDA QMSR
  • ISO 13485
  • EU MDR
  • IVDR
  • MDSAP

Nutraceuticals

DSHEA + 21 CFR Part 111 GMP for US dietary supplements; EFSA novel-food authorization (EU 2015/2283, updated 2024) for EU market access.

  • FDA DSHEA
  • 21 CFR Part 111
  • NSF/ANSI 173
  • EFSA
  • EU Novel Food

Cannabis & hemp

State seed-to-sale + Health Canada CTR + USDA Hemp. Federal hemp redefinition (Nov 2026 — 0.4mg THC cap) reshaping US market; EU treats CBD as Novel Food.

  • US state cannabis
  • Health Canada CTR
  • USDA Hemp
  • EU Novel Food (CBD)

Animal feed

FAMI-QS for specialty ingredients; FSMA Animal Food + EU 183/2005 for hygiene; ISO/TS 22002-6 prerequisite programs aligned with HACCP.

  • FAMI-QS
  • FSMA Animal Food
  • EU 183/2005
  • ISO/TS 22002-6

Water treatment

NSF/ANSI 60 (added chemicals) + NSF/ANSI 61 (system components). EU 2020/2184 risk-based approach (full effect 2027); EPA SDWA transitioning to LCRI (lead) and CCL 6 (microplastics).

  • NSF/ANSI 60
  • NSF/ANSI 61
  • EU 2020/2184
  • EPA SDWA
  • WHO Guidelines

Chemicals & petrochemicals

REACH + CLP (EU) and TSCA (US), both aligned to UN GHS Rev. 7. OSHA HCS deadline Nov 2026 — substantial labelling and SDS changes.

  • REACH
  • EU CLP
  • GHS Rev. 7
  • OSHA HCS
  • TSCA

Agriculture & farming

Primary production through organic certification. EU Organic equivalence model sunsets Dec 2026 — non-EU producers move to full compliance with EU 2018/848.

  • GLOBALG.A.P.
  • EUDR
  • USDA Organic
  • EU 2018/848

Packaging

Food-contact + packaging waste. PPWR (EU 2025/40, Aug 2026) introduces PFAS limits; no grandfathering of inventory.

  • EU 1935/2004
  • FDA Food Contact
  • BRCGS Packaging
  • PPWR (EU 2025/40)

Electronics & manufacturing

Restricted substances + ecodesign. EU Battery Regulation mandates QR + DPP from Aug 2026; ESPR DPP follows for other electronics from 2027.

  • ESPR
  • EU Battery Regulation
  • RoHS
  • REACH
  • WEEE

Fashion & textiles

Fibre-to-garment chemical safety + ecodesign. EU Textile EPR (2027) and ESPR delegated act drive material disclosure; ZDHC MRSL and OEKO-TEX certify supply-chain inputs.

  • BCI
  • GOTS
  • OEKO-TEX
  • ZDHC MRSL
  • ESPR Textiles

Mining & raw materials

Mine-to-mill responsible sourcing. EU CRMA accelerating strategic materials supply; OECD due-diligence + EU Conflict Minerals shape import compliance for 3TG.

  • IRMA
  • OECD Due Diligence
  • EITI
  • EU CRMA
  • EU Conflict Minerals

Logistics & supply chain

Cross-border + cold-chain compliance. AEO + C-TPAT for customs; ISO 28000 unifies security management; GDP and FSMA Sanitary Transport for temperature-sensitive goods.

  • AEO
  • C-TPAT
  • ISO 28000
  • FSMA Sanitary Transport
  • GDP

Retail & e-commerce

Consumer data + product safety + platform obligations. GDPR + PCI DSS for data and payments; GPSR (Dec 2024) for product safety; DSA for platform conduct.

  • GDPR
  • PCI DSS
  • EU GPSR
  • FTC labelling
  • EU DSA

Hospitality & tourism

Food service + guest data. HACCP and ISO 22000 for kitchens; GDPR and PCI DSS for guest information and payments.

  • HACCP food service
  • ISO 22000
  • GDPR
  • PCI-DSS

Automotive

QMS + functional safety + supply-chain due diligence. IATF 16949 (built on ISO 9001), ISO 26262 for functional safety, CSDDD for tier-2+ visibility.

  • IATF 16949
  • ISO 26262
  • ELV Directive
  • CARB
  • EU CSDDD

Aerospace & defence

AS9100D for QMS + NADCAP for special processes. ITAR + EAR + DFARS for export control and DoD-cleared supply chains; NIST 800-171 / CMMC where defence contracts require.

  • AS9100
  • NADCAP
  • ITAR
  • EAR
  • DFARS

Construction & building

Construction-product compliance + green-building. EU CPR 2024/3110 (active Jan 2026 — replaces 305/2011) requires EPDs aligned to EN 15804+A2; BREEAM/LEED for whole-building rating.

  • EU CPR 2024/3110
  • BREEAM / LEED
  • EPD ISO 14025
  • EN 15804+A2

How we choose what to cover — 80+ frameworks, edited with intent.

Coverage breadth matters, but so does editorial integrity. The frameworks above reflect what operators actually have to comply with in 2026 — not a long tail of tangential standards. Here's how we curate the list.

  1. 1.

    Active frameworks only: When a framework supersedes another (FDA QMSR replaced 21 CFR 820 in Feb 2026; EU CPR 2024/3110 replaces 305/2011 from Jan 2026), we show the successor. The old citation lives in the subtitle for context.

  2. 2.

    Frameworks, not trade bodies: Voluntary industry guidance (e.g., CTPA for UK cosmetics, ZDHC certifications) appears in subtitle context where it materially shapes compliance posture — but we don’t chip it as a framework.

  3. 3.

    Emerging regulations tracked: PPWR (Aug 2026), EU Battery DPP (Aug 2026), federal hemp redefinition (Nov 2026), EU Organic equivalence sunset (Dec 2026), OSHA HCS Rev. 7 (Nov 2026) — included with effective dates so customers can plan.

  4. 4.

    No double-listing derivatives: ISO 9001 is the QMS foundation underneath IATF 16949 (auto), AS9100 (aerospace), and many others. We chip the derivative since it includes and extends ISO 9001 — not both.

  5. 5.

    Per-industry depth, not breadth padding: Each card lists the 4-6 frameworks an operator in that sector actually has to comply with — not adjacent standards. Cosmetics doesn’t need REACH on its card just because some ingredients touch it.

  6. 6.

    Cross-jurisdiction by default: Where US, EU, and international frameworks address the same control, all three appear. Submission outputs are format-native per regulator (47 country regulators covered, see Regulators section).

Audit-week timeline

From audit notice to renewed cert. 8.5 hours of team time.

A real BRCGS Issue 9 cycle. Pre-Traceage, this same audit consumed 3-4 weeks of QA team time. With Traceage, evidence assembly is automatic and the team-hours line item drops to a single afternoon.

  1. Day -14

    Audit notice received

    BRCGS auditor confirms on-site visit. Traceage compiles the in-scope CCP set, doc-control versions, and supplier evidence into the audit packet automatically.

  2. Day -10

    Evidence preview

    QA lead reviews the auto-assembled evidence pack. Flags two open SAQs and one expired pest-control inspection — addressed inside the platform, not in email.

  3. Day -3

    Final packet locked

    All evidence ready. Composite readiness score hits 100%. Audit packet exported as PDF + signed bundle. Total preparation time across the team: 6.5 hours.

  4. Day 0

    Auditor on-site

    Auditor logs in via the scoped read-only portal. Walks the floor against pre-mapped CCPs. Pulls citations live; no scrambling for missing artefacts.

  5. Day +2

    Findings issued

    Two minor non-conformances logged as findings. Both trigger CAPA workflows directly inside Traceage — no external tracker, no double-keying.

  6. Day +14

    Recertified

    BRCGS Issue 9 certificate renewed. Renewal date set to Day +365; renewal-aware reminders begin firing at Day +335. Total team-hours: 8.5.

Compare by plan

Compliance is in every plan. Frameworks and KYC/KYB scale with you.

CapabilityStarterGrowthPremiumEnterprise
Automated compliance monitoring
IncludedIncludedIncludedIncluded
GFSI standards (BRCGS / SQF / FSSC 22000)
IncludedIncludedIncludedIncluded
Evidence library
IncludedIncludedIncludedIncluded
Regulatory submission generation
LimitedIncludedIncludedIncluded
Audit scheduling & tracking
IncludedIncludedIncludedIncluded
Document control & versioning
LimitedIncludedIncludedIncluded
Multi-framework support
LimitedIncludedIncludedIncluded
Custom framework mappingComing soon
Not includedNot includedIncludedIncluded
EUDR / deforestation pack
Coming soon
Not includedNot includedIncludedIncluded
KYC / KYB
Coming soon
Not includedIncludedIncludedIncluded

See full pricing breakdown

Pairs well with

Related capabilities.

HACCP automation

HACCP plans, CCPs, PRPs, and deviation-to-CAPA all feed directly into your compliance evidence library. No separate food-safety system to maintain.

Learn more

Supplier management

Supplier SAQs, KYC/KYB results, and certificates roll into BRCGS, SQF, FSSC 22000 audit packets without re-entry.

Learn more

Digital Product Passport

ESPR-driven DPP compliance leverages the same multi-framework engine. Audience views and visibility layers are framework-aware.

Learn more
Private beta now open

Stop running compliance on a parallel system.

20 industries · 80+ frameworks · 47 countries · audit-week prep in hours, not weeks.

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