How to use AuditCore

Step-by-step guidance for every part of the platform — from onboarding to BRC-aligned reporting. Use the search or navigate by section.

Platform overview

AuditCore is a cloud-based internal audit and compliance platform for food manufacturing and processing. It covers two disciplines in one system: food safety, aligned to BRC Global Standard Issue 9 and the other GFSI-recognised schemes, and health & safety, aligned to ISO 45001 and HSG65. A site can run either or both.

ℹ AuditCore centralises the entire audit lifecycle — from risk-based scheduling to verification of corrective actions — giving you a single, timestamped record for audit day. Food safety and health & safety findings share one non-conformance register and one CAPA process, so you are not running two systems side by side.

Who uses AuditCore

Quality & Technical

Define the annual audit programme, oversee NC trends, and generate evidence-led reports for management review.

Auditors & Site Managers

Execute shopfloor GMP inspections and structured system audits with photo evidence and clause references.

Operations & Production

Primary owners of the CAPA process — responsible for immediate corrections and root cause investigations.

Senior Management

Monitor real-time site health via the Risk Heatmap to satisfy BRC Clause 1.1.2 resource and management review requirements.

Health & Safety

Run safety tours and ISO 45001 or HSG65 audits on the same site, with findings landing in the same NC register as food safety.

Pre-loaded audit standards

The following standards are available from the moment your site is created. Which of them you are offered depends on what you told us the site audits:

  • BRC Global Standard for Food Safety Issue 9
  • FSSC 22000 v6
  • IFS Food v8
  • SALSA Issue 6
  • SQF Edition 9
  • ISO 45001 — occupational health & safety management systems
  • HSG65 — the HSE's Plan, Do, Check, Act framework

Organisations & sites

AuditCore uses a strict three-level hierarchy to maintain data integrity and clear segregation of duties across complex business units.

Hierarchy

  • Organisation — the top-level legal entity. Subscription settings and master GMP templates are managed at this level.
  • Site — a physical factory or warehouse. All data (audits, NC registers, risk scores) is scoped to a specific site.
  • Areas — specific locations within a site (e.g. "High-Care Packing" or "Raw Material Intake") used to pinpoint where an observation or failure occurred.

Site profile

During onboarding each site completes a profile which informs the risk assessment engine and report headers, and records which disciplines it audits.

FieldDescription
Site NameUnique identifier, e.g. "BAKM — Manchester Bakery"
Production AreasTotal count of defined functional zones within the facility
Employee CountStaffing levels used to contextualise the scale of operations
High-care FlagBoolean indicator of whether the site contains high-care or high-risk production environments
What this site auditsFood safety, health & safety, or both. Decides which standards are offered and which registers appear. Changed later in Settings → Site Settings

Managing production areas

Areas are managed via Settings → Sites → [Site Name] → Areas. Precise area definition is critical for the evidence trail required by auditors.

  • Area types: Production, Storage, Despatch, Welfare, Utilities, or Other
  • High-care status: A toggle to identify zones requiring enhanced hygiene and segregation controls
  • Status & order: Admins can set areas to Active/Inactive (hiding defunct areas without losing historical data) and adjust sort order for auditor efficiency

User roles

AuditCore uses an additive permission model. Each successive role inherits all permissions of the roles below it, ensuring a clear chain of command and data security. There are four roles — there is no separate "auditor" role, because conducting audits is what site users and site managers already do.

RolePrimary permissionsKey restrictions
site_user View the dashboard and My Work; conduct assigned inspections and system audits; raise non-conformances; complete assigned CAPA phases; log Proactive Actions Restricted to their assigned site(s). Cannot build or schedule programmes, manage inspection templates, or access site and organisation settings
site_manager All site_user permissions plus: build and schedule programmes; reassign audits; manage inspection templates, areas and site settings; view site reports Restricted strictly to their assigned site(s)
org_admin All site_manager permissions plus: every site in the organisation; invite and deactivate users; organisation settings and billing; run manual risk assessments Cannot access data from other organisations (multi-tenancy lock)
super_admin All org_admin permissions plus: support-level access; log in on behalf of users; global organisation management Reserved for AuditCore technical service team only
⚠ When a user leaves the organisation, deactivate rather than delete their account. This preserves the full audit trail — their name remains on all historical audits and NCs they conducted or verified.

Two-factor authentication

Any user can protect their own account with an authenticator app, whatever their role — see Security & 2FA. It is worth insisting on for org admins, who can see every site in the organisation.

What roles do not control

The Focus switcher between food safety and health & safety is a view filter, not a permission. Everyone working on a site sees the disciplines that site runs; who may build a programme or assign work is governed by the roles above.

Onboarding & setup

New accounts start with a 14-day full-access trial. Signing in for the first time takes you straight into setup — you come out of it with a real audit programme for the year rather than an empty dashboard.

Onboarding wizard

  1. Your site — the site name that appears on every report and NC reference
  2. What you audit here — food safety, health & safety, or both. This decides which standards you are offered and which registers you see, and you can change it later in Settings
  3. High care / high risk — flags the zones that need tighter controls during inspections
  4. Your standard and schedule — pick from BRC Issue 9, FSSC 22000, IFS, SQF, SALSA, ISO 45001 or HSG65, choose when your cycle starts, and AuditCore drafts the year's audits
  5. Your team — invite the colleagues who will run the audits

Only the person who created the account goes through setup. Colleagues invited afterwards join a site that is already configured and land straight on the dashboard.

Account states

  • Trial — 14-day full-access period for new registrations
  • Active — live paid subscription; full platform access
  • Expired — subscription lapsed; login blocked until renewed
  • Suspended — account suspended based on payment status

GMP inspections

Inspections are checklist-based walk-rounds. For food safety they evaluate Prerequisite Programmes — hygiene, maintenance, pest control and so on. For health & safety they are safety tours covering fire, machinery, COSHH, work at height and the rest. Both use the same screens, the same evidence capture and the same route into the NC register. In the app they are under Inspections, with the checklists themselves under Inspection Templates.

Conducting an inspection

  1. Select the template for the area you are inspecting — the list shows the checklists for the disciplines your site runs, plus any your organisation has created
  2. Mark each item as Pass, Fail, or N/A
  3. For any failure: add notes and up to 5 photos as evidence
  4. Record the Area, Shift, and Product Reference in the metadata fields
  5. On failing an item, use the Auto-NC button to immediately raise a linked Non-Conformance

Inspection templates

AuditCore ships 17 checklists: eight GMP templates for food safety and nine safety tours for health & safety. These are built in and shared by every customer, so they cannot be edited — copy one and adjust the copy if you want your own wording.

Templates you create belong to your organisation and are visible only to it. Org admins and site managers manage them under Inspection Templates.

Offline support

AuditCore uses Service Workers and local caching to support audits in Wi-Fi dead zones — cold stores, external yards, or areas with poor signal.

✓ The Ready Offline badge confirms the template and site data are cached to your device. Responses save locally and sync automatically once a stable connection is restored.

System audits

System audits evaluate the facility against the full breadth of a standard, clause by clause — BRC, FSSC 22000, IFS, SQF and SALSA for food safety, ISO 45001 and HSG65 for health & safety. They can be scheduled via the Audit Programme or raised as one-off or triggered audits.

Audit lifecycle

  1. Schedule — create manually or let the Audit Programme generate it automatically
  2. Execute — work through clauses using the Audit Mode: Desk, Shopfloor, Interview, or Combined
  3. Report — on completion a PDF generates automatically with overall compliance score, embedded photo evidence, and a summary NC table

Audit modes

ModeUse case
DeskDocument review — procedures, records, HACCP plans
ShopfloorPhysical walkthrough of the production environment
InterviewStaff competency and awareness checks
CombinedMixed approach covering all of the above in a single audit session

Triggered audits

Outside the routine plan, triggered audits are initiated by specific events:

TriggerExample case
Customer ComplaintSignificant complaint requiring a deep-dive audit response
Product RecallAudit conducted as part of a formal recall or withdrawal
Post-IncidentConducted following a food safety incident or near-miss
Process ChangeTriggered by new line installations or process modifications
Supplier FailureTargeted audit following a significant supplier non-conformance
ℹ Audits can be flagged as Unannounced to help meet BRC Issue 9 requirements for unannounced internal audit proportions.

Health & safety audits

AuditCore runs health & safety alongside food safety, in the same programme, with the same non-conformance and CAPA workflow. A site can do one or both.

Turning it on

Setup asks what you audit at each site. If you did not pick health & safety then — or you have added it since — go to Settings → Site Settings and switch it on. Turning a discipline off hides its work; it never deletes anything.

Standards

  • ISO 45001 — occupational health & safety management systems, 21 sections and 81 clauses
  • HSG65 — the HSE's Plan, Do, Check, Act framework, 12 sections and 56 clauses

Safety inspections

Nine walk-round checklists ship with the platform, written against UK duties and phrased as things an inspector can see on the floor rather than documents to request:

  • General Workplace Safety Tour
  • Fire Safety — escape routes, fire doors, extinguishers
  • Machinery & Guarding (PUWER)
  • Manual Handling
  • COSHH & Chemical Storage
  • Work at Height
  • Slips, Trips & Falls
  • PPE Compliance
  • Welfare Facilities

They work exactly like GMP inspections — same five response types, same photo and voice evidence, same route into the NC register.

Switching between disciplines

A site running both gets a Focus switcher in the sidebar: All, Food Safety, or Health & Safety. It filters every register, dashboard figure and report at once, so a safety manager can work without wading through food-safety records and vice versa. A site running only one discipline does not see the switcher at all.

Non-conformances

H&S findings raise non-conformances in the same register, tagged with an H&S badge, and follow the same corrective action, root cause and verification steps. One CAPA process for the whole site, not two.

NC & CAPA process

Every Non-Conformance in AuditCore follows a mandatory two-phase CAPA workflow. Unlike Proactive Actions — which are simple improvement logs requiring no formal verification — every NC must complete a structured, multi-stage process.

Who can raise one

Anyone can raise a non-conformance against a site they are assigned to — an operator who spots a problem should be able to log it without going through a manager. Org admins can raise one against any site in the organisation. Nobody can raise one against a site they do not work at.

NC reference format

Each NC is assigned a unique reference following the format: NC-{SITE}-{YEAR}-{SEQUENCE} (e.g. NC-BAKM-2026-0001). The site code is automatically generated from the first four characters of the site name, uppercase, no spaces.

Food safety and health & safety

Non-conformances carry a FOOD or H&S badge according to the audit or inspection that raised them, and sit in the same register. The Focus switcher filters the register to one discipline when you want to work on it alone. The CAPA workflow itself is identical for both.

NC source types

SourceDescription
System AuditAuto-raised during internal audits against certification clauses
External AuditFindings from third-party or certification body visits
GMP InspectionAuto-raised from a failed shopfloor inspection item
Customer ComplaintFormal feedback requiring a technical response
IncidentFood safety incidents or near-miss events
Non-Conforming ProductProduct failing specification or release criteria
Product Safety Point FailureFailure of a CCP, OPRP, or other HACCP control
Cleaning FailureDocumented failure of cleaning and disinfection protocols
Supplier IssueNon-conformance regarding delivery or supplier performance
Internal (Other)Internally identified issues not covered by other sources
Manual / Ad HocA manually created record for miscellaneous compliance failures

Severity levels & due dates

SeverityDefinitionDue date
CriticalImmediate risk to safety or legalitySame day
MajorSubstantial failure or potential risk3 days
MinorFailure not posing significant immediate risk14 days
ObservationWeakness or area for improvement30 days

The three-step CAPA workflow

  1. Phase 1 — Immediate correction. Document what was done immediately to prevent harm (e.g. "Batch isolated and quarantined"). Assign a Corrective Action Owner.
  2. Phase 2 — Root cause investigation & prevention. Record a Root Cause Analysis using methods such as the 5 Whys or Fishbone diagram. Then document the Preventive Action Plan that addresses the root cause finding.
  3. Verification & closure. A different person from the submitter must verify the actions taken. They may close the NC or return it for rework if evidence is insufficient.
⚠ The verifier must be a different person from the submitter to maintain independence and satisfy BRC requirements for CAPA integrity. The only exception is single-person organisations.

Programme builder

AuditCore separates the library of audit requirements from the execution of the schedule. The Programme Builder defines what needs to be audited and how often. The Annual Plan puts those requirements on the calendar.

Programme builder vs annual plan

ToolPurposeAnswers
Programme BuilderThe master library of Audit EventsWhat needs auditing, how often, and at what baseline risk level
Annual PlanThe site-specific 12-month calendarWhen each audit event is actually scheduled throughout the year
ℹ You do not need to set up Programme Builder before you can audit. You can schedule a one-off system audit directly from the System Audits page. Programme Builder is recommended for managing a structured, risk-adjusted annual programme.

Building a programme quickly

Build programme for me starts you from a ready-made programme for the chosen standard — a sensible division of its clauses into named audits — which you then rename, re-risk and reschedule. It is a starting point, not a commitment; nothing is scheduled until you say so.

Clause coverage

As you assign clauses to events, the builder shows what percentage of the standard your programme reaches and lists the clauses it does not. The percentage tells you there is a gap; the list tells you what it is, which is what you need to close it.

Which site you are building for

The builder works on the site selected at the top of the page. Switch site there and the events, coverage and standards all follow.

Using the annual plan view

The Annual Plan View displays a 12-month grid. Quality Managers use it to schedule specific instances of Programme Builder events, ensuring even distribution of workload and audit coverage across the year.

Risk assessment engine

In accordance with BRC Clause 3.4, AuditCore automatically calculates compliance risk at the section level — rated High, Medium, or Low — using a multi-factor scoring model.

Risk weighting factors

FactorImpact on score
Recent compliance scoreThe primary driver of current section risk
Number of open NCsIncreases risk based on volume of unresolved issues
Overdue NCsSignificant negative factor indicating lack of control
Repeat NCsHigh-priority flag — triggered when the same clause fails in two or more consecutive audits
Time since last auditRisk increases linearly as the duration since the last check grows
✓ The Risk Heatmap on the dashboard provides an early warning system, allowing management to increase audit frequency for sections flagged as High Risk before the next BRC visit.

Reports & exports

AuditCore generates two primary reports designed to meet BRC Issue 9 evidence requirements and support management review.

Management review report

Directly supporting BRC Issue 9 Clause 1.1.2, this report provides Senior Management with the data required to review the effectiveness of the Food Safety Quality Management System.

  • NC trends by severity
  • Open vs. closed rates
  • Average time to close
  • Repeat NC list
  • Audit completion rates
  • Risk score trends over time

Report activity

Every management review and NC register you generate is recorded, and the Reports page lists the recent ones so you can see what has already been produced and when.

NC register export

Exports follow the site and date range selected on the Reports page — check the site is the one you mean before generating a file you intend to send to a customer or an auditor. The full register can be exported in two formats:

  • CSV — for internal data manipulation and trend analysis
  • PDF — a professionally formatted register suitable for direct submission during certification audits

System audit PDF

Generated automatically on audit completion. Includes the overall compliance score (percentage of compliant non-N/A responses), all embedded photo evidence, and a summary NC table.

Security & two-factor authentication

Your audit records, non-conformances and reports sit behind one password by default. Two-factor authentication adds a code from your phone, so a stolen password is not enough on its own.

Turning it on

  1. Go to Settings → Security
  2. Press Set up two-factor authentication
  3. Scan the QR code with any authenticator app — Google Authenticator, Microsoft Authenticator, 1Password, Authy. If your camera will not scan, the key is shown for typing in by hand
  4. Enter the 6-digit code the app shows. Nothing is switched on until a code works, so a QR scanned into the wrong app cannot lock you out
  5. Save the eight recovery codes

Recovery codes

Shown once, immediately after you turn 2FA on, and never again. Each works a single time and they are the way back in if you lose your phone — so keep them somewhere other than the phone running the authenticator app. A password manager or a printout in a drawer both work.

Settings → Security shows how many you have left and warns you when you are down to two.

Signing in afterwards

Email and password as usual, then a second step asking for the 6-digit code. If you have not got your phone, choose Use a recovery code instead. Codes are accepted for thirty seconds either side of their window, so a phone clock slightly out of sync still works.

Turning it off

Settings → Security → Turn off. Your password is required, so somebody who finds your screen unlocked cannot quietly remove it.

Who should use it

Anyone can turn it on for their own account. We would strongly recommend it for org admins, who can see every site in the organisation.

Sample data

New accounts are seeded with a handful of example non-conformances and proactive actions so the dashboard shows a working product rather than empty states on day one.

Spotting it

Everything seeded is titled "Sample — …" and carries an NC-DEMO reference. Nothing you create is ever marked that way.

Clearing it

Go to Settings → Sample Data. It shows how many example records remain, split by type, and removes them in one step. Only rows flagged as sample data are deleted — your own records are untouched. A banner on the dashboard and the NC register offers the same thing until the examples are gone.

Clearing is permanent and cannot be undone, so do it once you have had a look round and are ready to work with real records.

Video walkthroughs

Short screencasts covering the key workflows in AuditCore. More videos will be added as the product develops.

Building and Scheduling the Audit Programme
How to use the Programme Builder to define audit events and the Annual Plan to schedule them across the year.
5 min · Programme Builder & Annual Plan

FAQ & troubleshooting

Common questions from Technical Managers getting started with AuditCore.

Yes. ISO 45001 and HSG65 audits, plus nine safety-tour checklists covering fire, machinery, COSHH, manual handling, work at height and more. Findings go into the same non-conformance register and follow the same CAPA process as food safety. A site can run one discipline or both — see Health & safety audits.
The Focus switcher only appears on a site that runs both disciplines, because there is nothing to switch between otherwise. Go to Settings → Site Settings and check what the site is set to audit. Turning a discipline on there makes the switcher appear straight away; turning one off hides its work rather than deleting it.
Everything seeded with a new account is titled "Sample — …" with an NC-DEMO reference. Clear it in one step from Settings → Sample Data, or from the banner on the dashboard. Only sample rows are deleted; your own records are untouched.
Use one of the recovery codes you saved when you turned two-factor authentication on. At the code prompt, choose Use a recovery code instead. Each code works once. Once you are back in, go to Settings → Security, turn 2FA off and set it up again on the new phone. If you have run out of recovery codes, contact us.
Some company mail servers scan every link in an incoming email before you see it, which can use up a single-use confirmation link. Your account is almost certainly already confirmed — try signing in. If it still refuses, use "Forgot password" or get in touch and we will sort it out.
No. You can schedule a one-off system audit directly from the System Audits page. Programme Builder is recommended when you want to manage a structured, risk-adjusted annual programme with automatic scheduling and frequency controls.
Only in single-person organisations. In all other cases, the verifier must be a different person from the submitter. This is a BRC requirement for CAPA integrity and AuditCore enforces it at the point of verification.
The platform works offline. When you open a GMP inspection template on a device with a connection, the template and site data are cached locally. If you lose signal mid-inspection, your responses continue to save to the device. Data syncs automatically once a stable connection is restored.
BRC Global Standard for Food Safety Issue 9, FSSC 22000 v6, IFS Food v8, SQF Edition 9, and SALSA Issue 6. All are available from the moment your site is created.
No. Deactivate the account rather than deleting it. This preserves the full audit trail — their name remains attributed to all historical audits and NCs they conducted or verified, which is required for BRC evidence purposes.
Each NC is assigned a unique reference in the format NC-{SITE}-{YEAR}-{SEQUENCE}. For example, NC-BAKM-2026-0001. The site code is automatically generated from the first four characters of the site name (uppercase, no spaces). Sequence numbers increment per calendar year.
A Proactive Action is a simple log for continuous improvement observations — it does not require formal verification or a two-phase CAPA workflow. An NC is a formal non-conformance that requires immediate correction, root cause investigation, preventive action, and independent verification before it can be closed.
The Risk Heatmap on the dashboard shows compliance risk rated High, Medium, or Low at the BRC section level. Risk is calculated from five factors: recent compliance score, open NC count, overdue NCs, repeat NCs, and time since last audit. Sections flagged High Risk should be prioritised for increased audit frequency before the next BRC visit.

Try AuditCore free for 14 days.

No credit card. No demo. Full access from day one.

Start Free Trial