HACCP Dietary Supplements Management System
HACCP Dietary Supplements Management System
In supplement manufacture the two things that can never go wrong are what goes into the blend and what goes onto the label.
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Written and reviewed by practising specialists. Who writes this
Built and reviewed with our methodology. Read it
By document type
| Category | Files |
|---|---|
| Manuals | 10 |
| Policies | 1 |
| Procedures & SOPs | 38 |
| Plans & Programmes | 1 |
| Forms & Records | 49 |
| Checklists & Audit Tools | 19 |
| Registers, Logs & Matrices | 1 |
| Training & Awareness | 24 |
| Guides & Work Instructions | 18 |
Key documents
| Reference | Document | Format |
|---|---|---|
| AGS-SUP-MAN-001 | HACCP Quality Manual | Word |
| AGS-SUP-PLN-001 | Dietary Supplements HACCP Plan & Study | Word |
| AGS-SUP-PRO-026 | CCP Management & Monitoring | Word |
| AGS-SUP-PRO-029 | Labelling & Artwork Control | Word |
| AGS-SUP-FRM-047 | Hazard Analysis Worksheet | Word |
| AGS-SUP-FRM-049 | Critical Limits Register | Word |
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Overview
Built on Codex Alimentarius CXC 1-1969 Rev. 2023 and its seven principles and twelve steps, this HACCP management system is written for dietary supplement manufacturing across tablets, capsules, powders, sachets and liquids. Its hazard analysis defines CCP-1 metal detection, with validated ferrous, non-ferrous and stainless-steel sensitivity plus functional reject-device verification, and CCP-2 labelling and label reconciliation, held to a full label-to-artwork match. Operational prerequisite programmes sit beneath them at raw material receipt, dispensing and blending, granulation and drying, and seal integrity.
That shape follows the failure modes the sector actually suffers — mix-ups, mislabelling, foreign bodies, and inconsistent moisture or blend uniformity — rather than generic food hygiene. The framework layer sets out prerequisite programmes, hazard analysis and CCP determination, verification and validation, traceability and recall, and training and competence, while the SOPs reach into artwork control, foreign body control, and site security and product defence. The record library matches that depth: blend uniformity, drying and moisture (LOD), seal integrity, line clearance and label reconciliation, and metal detection monitoring each have their own editable Word form. Critical limits arrive as provisional values for your own validation to confirm.
What this system covers
- Raw material receipt, supplier approval and incoming release testing
- Dispensing, weighing and blending — line clearance, blend uniformity and mix-up prevention
- Granulation and drying — loss-on-drying evidence and in-process moisture limits
- Metal detection (CCP-1) — Fe, non-Fe and stainless sensitivity, and reject-device function
- Labelling, artwork control and label reconciliation (CCP-2)
- Packing and seal integrity — closure checks and dispatch release
- Allergen management, cleaning and sanitation, and cross-contamination prevention
- Traceability, withdrawal and recall, with site security and product defence
Who it's for
Tablet, capsule, powder and liquid supplement manufacturers, contract manufacturers included, facing a GMP or HACCP audit, a new retail listing or an export customer's technical questionnaire. It suits the quality lead who inherited a plant with real controls and thin paperwork; afterwards the hazard study, the CCP monitoring records and the verification evidence line up when an auditor reads them in order.
Everything you get
Every toolkit gives you a full set of working documents for your standard, ready to edit and use.
Native Microsoft files. Add your logo and adapt every document to how you work.
Your full toolkit arrives as a ZIP the moment payment clears.
One purchase covers everyone in your organisation. No per-seat fees.
Built by people who run real audits, so the content matches what assessors check.
One payment, perpetual licence for your organisation. No subscriptions, no renewals.
Full refund if your files are faulty, incomplete or not as described and we can't put it right
Frequently asked questions
What exactly do I receive?
A downloadable ZIP containing the full set of ready-to-use documents for this toolkit — manuals, procedures, forms, records, checklists, guidance and training material, all in editable Word and Excel format. The exact document count is shown at the top of this page.
Are the documents really editable?
Yes. Every file is native Microsoft Word or Excel — no locked PDFs. Add your logo, change wording, and tailor the content to your organisation. The toolkit is yours to keep and reuse.
Does this certify my organisation?
No. These are documentation toolkits aligned to the relevant standard to help you prepare. Certification itself is issued by an accredited certification body after their audit. Our toolkits give you a strong, audit-ready starting point.
How is it delivered?
Instantly and digitally. There's no physical shipment — you download the files right after payment and receive a backup link by email.
Do I get updates?
Yes. If we revise this toolkit, you're entitled to the updated version at no extra cost — just contact us with your order details.
What is your refund policy?
These are digital products, so once a toolkit has been downloaded we cannot take it back. If you have not downloaded yet, contact us and we will cancel the order and refund you in full. We also refund in full if the files are damaged, incomplete, or not what the product page described.
Cannot find your standard?
Tell us which scheme you work to. We will point you to the right toolkit.
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