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Explore all industries
    • Bakery & Confectionery
    • Food Processing
    • Ingredients & Dry Mixes
    • Sausage & Meat Products
    • Produce Packing
    • Pet Food & Pet Supplements
    • Dairy & Chilled Foods
    • Beverages & Liquid Manufacturing
    • Infant Formula
    • Radiopharmaceuticals
    • Pharmaceutical
    • Medical Devices
    • Veterinary Pharmaceuticals
    • Blood & Tissue
    • Diagnostics & IVD Kits
    • Reference Materials & Standards
    • OTC Topical Creams & Gels
    • Dietary Supplements
    • Cosmetics & Personal Care
    • Cannabis & Hemp Manufacturing
    • Fragrances & Perfumery
    • Soaps & Personal Hygiene
    • Botanical Extracts & Essential Oils
    • Plastics & Resins
    • Agricultural Chemicals
    • Specialty & Industrial Chemicals
    • Printing Inks, Pigments & Construction Chemicals
    • Lubricants & Metalworking Fluids
    • Coatings, Adhesives & Sealants
    • Consumer Products
    • Electronics & Electrical Assembly
    • Textiles & Nonwoven
    • Contract Manufacturing & Co-Packing
    • Packaging & Food-Contact Materials
    • Regulated Warehousing & Distribution
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Hazard analysis · CCPs · Verification · Corrective action

HACCP software for UK food manufacturers.

Record CCP checks against your limits, with out-of-limit results surfaced for a person to act on.

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  • Critical Limits Enforced, Not Suggested

    A reading outside the critical limit blocks the next step, opens the deviation and notifies the responsible person in the same action.

  • Monitoring captured at the point and time of check

    Tablet or kiosk entry with operator identity, timestamp and equipment reference.

  • Verification, Validation and Review Evidenced

    Scheduled verification activities, calibration of monitoring devices, and change-triggered re-validation of the plan all carry records and signatures.

What goes wrong today3 common problems
  • The Plan and the Practice Drift Apart

    The HACCP study says one thing; the line does another. The gap only surfaces at audit or after a complaint.

  • CCP checks get signed in batches

    Ten checks signed at the end of a shift is not monitoring — and auditors can spot it from the timestamps.

  • Verification and annual review are a scramble

    Evidence that the plan was verified, reviewed and re-validated after change is scattered across emails and minutes.

Everything V5 does here5 capabilities
  • Critical Limits Enforced, Not Suggested

    A reading outside the critical limit blocks the next step, opens the deviation and notifies the responsible person in the same action.

  • Monitoring captured at the point and time of check

    Tablet or kiosk entry with operator identity, timestamp and equipment reference. Missed checks escalate live.

  • Verification, Validation and Review Evidenced

    Scheduled verification activities, calibration of monitoring devices, and change-triggered re-validation of the plan all carry records and signatures.

  • Corrective Action with Root Cause

    Product disposition, root cause, action, owner, due date and effectiveness check — the chain the auditor follows.

  • Works Alongside BRCGS, SALSA and FSSC

    One HACCP record set, mapped to whichever scheme is auditing you this quarter.

Standards Referenced
  • Codex Alimentarius HACCP — seven principles
  • Retained EC 852/2004 Article 5
  • BRCGS Issue 9 clause 2 (HACCP / food safety plan)
  • UK Food Safety Act 1990 due-diligence defence
Related Pages
  • Food Processing
  • Sausage & Meat Products
  • Pet Food
  • Quality Management
  • Calibration Management
  • MES
  • HACCP
  • CCP
  • Corrective Action
Common questions4 answers
What is HACCP software?
Software that holds the hazard analysis and HACCP plan, enforces critical limits at each CCP as the process runs, records monitoring with attributable timestamps, and manages deviations, corrective actions, verification and plan review.
Does V5 stop production when a CCP fails?
It blocks the next step for the affected batch and opens a deviation with the lot, equipment, operator and reading attached. Product disposition is a controlled decision with a signature, not a verbal call.
How does it support the due-diligence defence?
Every monitoring record is attributable, time-stamped and tamper-evident, with the calibration status of the measuring device linked — which is what a due-diligence argument rests on.
Can we import our existing HACCP plan?
Yes. Existing hazard analyses, CCP tables and critical limits are configured into V5 during implementation; the plan is versioned from that point with change control.

Next Step

Try V5 with your own records, or ask a question first. Ask V5 opens with an editable question; nothing is sent until you choose to.

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V5 Ultimate
Ultimate

Warehouse, quality and manufacturing software for regulated operations.

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