ISO 22002-6 Toolkit – Feed & Animal Food Production PRPs

The toolkit is designed for feed mills, pet food manufacturers, premix and additive operations, animal food producers, feed safety teams, laboratories, internal auditors, and consultants implementing prerequisite programmes for feed and animal food production.

It includes editable Word procedures and plans, Excel registers, matrices and checklists, and PowerPoint review presentations covering governance, facilities, utilities, equipment, suppliers, receiving, storage, formulation, dosing, processing, carryover, medicated feed, contamination, sanitation, rework, release, dispatch, personnel, food defence, audit, and handover.

The supplied document register is organized into 19 implementation parts containing 143 templates. It progresses from enterprise governance and gap assessment through feed mill operations, formulation, processing, contamination control, product release, traceability, incident response, internal audit, corrective action, and enterprise handover.

Yes. The page provides a detailed document index so you can review the included file names and file types before purchase. The standard Index File, Payment Guide, and Free Sample options from the template page are retained.

Yes. ISO 22002-6:2025 is applied in conjunction with ISO 22002-100:2025. The supplied register includes combined requirements and internal audit tools for both the feed specific and common PRP requirements.

Yes. It includes facility layout, raw material and finished feed separation, zoning, access control, water and steam, ventilation, dust extraction, compressed air, equipment hygiene, preventive maintenance, line clearance, and calibration controls.

Yes. It includes supplier approval, raw material specifications, ingredient and additive registers, supplier reassessment, certificate of analysis tracking, and supplier and ingredient approval reviews.

Yes. It includes inbound vehicle and tanker inspection, ingredient receipt, sampling and testing, identification and traceability, quarantine, rejection, hold, and release controls.

Yes. It includes silo and bulk storage procedures, moisture and temperature monitoring, compatibility and species restrictions, FIFO and FEFO controls, silo cleaning, deterioration checks, and storage reviews.

Yes. It includes feed formula authorization, change control, inclusion limits, species compatibility, premix and micro ingredient dosing, weighing logs, formula revisions, and approval tracking.

Yes. It includes grinding, milling, mixing, pelleting, extrusion, start up, changeover, process parameters, mixing validation, heat treatment, cooling, drying, moisture control, and batch release.

Yes. It includes production sequencing, line cleanout, medicated and non medicated compatibility, species restricted ingredients, flushing verification, medicated feed authorization, carryover validation, and investigations.

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After payment is completed, the toolkit is provided through the site's download process. We recommend downloading the archive promptly and retaining a secure backup together with the purchase confirmation.

Yes. It includes mycotoxin and pesticide monitoring, Salmonella and microbiological testing, heavy metals, dioxin and other contaminants, sieves, magnets, foreign material verification, alert limits, trend reviews, and disposition decisions.

Yes. It includes dry sanitation, cleaning schedules and verification, pest monitoring and treatment, dust and spill controls, waste and by product handling, rework approval, compatibility, traceability, nonconforming feed, and disposal.

Yes. It includes finished feed sampling and testing, labels and species suitability, certificates of analysis, shelf life, packing, bagging, palletization, bulk loading, tanker hygiene, seals, delivery verification, and lot traceability.

Yes. It includes hygiene and facility entry, role based training, contractor and visitor controls, intentional contamination prevention, fraud vulnerability, incident investigation, traceability and recall exercises, PRP verification, internal audit, corrective action, KPIs, management review, and enterprise handover.

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