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Cosmetics GMP · ISO 22716:2007

ISO 22716:2007 Documentation Toolkit

A complete, editable ISO 22716:2007 documentation toolkit: a clause-by-clause manual, 38 procedures and 42 ready-to-use forms in Word and Excel, with sample filled examples.

1
Clause-by-clause
manual
38
Procedures
clause-mapped
42
Forms and records
with samples
2
Formats
Word and Excel
$149 Free sample
Within 24h secure delivery Editable Word and Excel Lifetime free updates
ISO 22716:2007MANUAL
Cosmetics GMP System Manual
Clause-by-clause structure
38Clause-mapped
procedures
42Ready-to-use
forms
Written to satisfy the requirements checked byBSISGSTÜVBureau VeritasDNVIntertek
Overview

Everything you need for ISO 22716:2007, in one download

Preparing the documentation is the slowest and most confusing part of getting certified to ISO 22716:2007. You have to work out what the standard asks for, decide what to write, and turn it into a manual, procedures and records that an auditor will accept. Done from a blank page it takes months, and paying a consultant to do it can cost thousands.

The ISO 22716:2007 Documentation Toolkit gives you that whole system, already written and ready to edit. It is built by practitioners around the exact structure of the standard, so nothing an auditor expects is missing. You add your company details, adapt anything specific to your operation, and you have a complete, consistent cosmetics gmp system that is ready for audit. Every single document you receive is listed and explained further down this page, so you know precisely what you are buying before you spend anything.

How the kit is built

Three tiers of documents that work together

Every kit follows the same proven structure, so it is easy to understand and easy to implement.

Tier 1

The Manual

The top level document. It answers ISO 22716:2007 clause by clause and sets out the scope of your system, your policy, the context of your organisation, and how your processes connect. This is the document an auditor opens first.

Tier 2

The Procedures

38 procedures that describe how you actually meet each requirement, from managing documents and training to internal audit and corrective action. They turn the manual into day-to-day practice.

Tier 3

The Forms and Records

42 ready-to-use forms and registers that capture the evidence an auditor wants to see. Sample filled forms are included so you can see exactly how each one is meant to be used.

The full contents

Every document in this toolkit, listed and explained

No hidden contents and no vague claims. Here is the complete document set, with a short description of what each file is for and the clause it helps you meet.

ISO 22716:2007 Toolkit

A complete document set, fully editable in Microsoft Office.

Manual1
Procedures38
Forms and records42
Total files81
Download free sample

ISO 22716:2007 System Manual

The top level document of the system, written clause by clause to match ISO 22716:2007. It states the scope, the policy, the context of the organisation, and how each requirement of the standard is met.

Introduction and scopeTerms and definitions4. Context of the organisation5. Leadership6. Planning7. Support8. Operation9. Performance evaluation10. ImprovementAnnexes: policy, process maps, list of procedures
PROC Procedures (38)
  • Procedure for Management review. Explains how top management reviews the quality system at planned intervals, what goes in, and what actions come out.
  • Procedure for Document and Data Control. Describes how document and Data Control is carried out and controlled to meet the requirements of ISO 22716:2007.
  • Procedure for Control of records. Describes how control of records is carried out and controlled to meet the requirements of ISO 22716:2007.
  • Procedure for Intemal Audit. Describes how intemal Audit is carried out and controlled to meet the requirements of ISO 22716:2007.
  • Procedure for Training. Describes how training is carried out and controlled to meet the requirements of ISO 22716:2007.
  • Procedure For Corrective and Preventive Action. Describes how corrective and Preventive Action is carried out and controlled to meet the requirements of ISO 22716:2007.
  • Procedure For Control of Monitoring and Measuring Equipment. Explains how measuring equipment is identified, calibrated, and maintained so the results you rely on stay valid.
  • Procedure for Purchasing. Describes how purchasing is carried out and controlled to meet the requirements of ISO 22716:2007.
  • Procedure for Control of Non-Conforming Products. Describes how control of Non-Conforming Products is carried out and controlled to meet the requirements of ISO 22716:2007.
  • Procedure for identification of products. Describes how identification of products is carried out and controlled to meet the requirements of ISO 22716:2007.
  • SOP for SOP. Describes how sOP is carried out and controlled to meet the requirements of ISO 22716:2007.
  • SOP for Control of Version, Archival and Retrieval of Data. Describes how control of Version, Archival and Retrieval of Data is carried out and controlled to meet the requirements of ISO 22716:2007.
  • SOP for Receipt and Handling of Market Complaints. Describes how receipt and Handling of Market Complaints is carried out and controlled to meet the requirements of ISO 22716:2007.
  • SOP for Product recall. Describes how product recall is carried out and controlled to meet the requirements of ISO 22716:2007.
  • SOP for Handling of market returns. Describes how handling of market returns is carried out and controlled to meet the requirements of ISO 22716:2007.
  • SOP for Change control system. Describes how change control system is carried out and controlled to meet the requirements of ISO 22716:2007.
  • SOP for Deviation and Investigation. Describes how deviation and Investigation is carried out and controlled to meet the requirements of ISO 22716:2007.
  • SOP for Vendor quality audit. Describes how vendor quality audit is carried out and controlled to meet the requirements of ISO 22716:2007.
  • SOP for Out of Calibration (OOC). Describes how out of Calibration (OOC) is carried out and controlled to meet the requirements of ISO 22716:2007.
  • SOP for Out of specification (OOS). Describes how out of specification (OOS) is carried out and controlled to meet the requirements of ISO 22716:2007.
  • SOP for Batch release of Finished Products. Describes how batch release of Finished Products is carried out and controlled to meet the requirements of ISO 22716:2007.
  • SOP for Rework procedure. Describes how rework procedure is carried out and controlled to meet the requirements of ISO 22716:2007.
  • SOP for In-process Inspection During Manufacturing. Describes how in-process Inspection During Manufacturing is carried out and controlled to meet the requirements of ISO 22716:2007.
  • SOP for Handling and storage of controlled samples. Describes how handling and storage of controlled samples is carried out and controlled to meet the requirements of ISO 22716:2007.
  • SOP for Retain samples and its disposal. Describes how retain samples and its disposal is carried out and controlled to meet the requirements of ISO 22716:2007.
  • SOP for Mock recall. Describes how mock recall is carried out and controlled to meet the requirements of ISO 22716:2007.
  • SOP for Receipt of Raw & Packaging Materials. Describes how receipt of Raw & Packaging Materials is carried out and controlled to meet the requirements of ISO 22716:2007.
  • SOP for Receipt, Storage& Dispatch of Finished Goods. Describes how receipt, Storage& Dispatch of Finished Goods is carried out and controlled to meet the requirements of ISO 22716:2007.
  • SOP for Waste management. Describes how waste management is carried out and controlled to meet the requirements of ISO 22716:2007.
  • SOP for Cleaning and sanitization. Describes how cleaning and sanitization is carried out and controlled to meet the requirements of ISO 22716:2007.
  • SOP for Pest control. Describes how pest control is carried out and controlled to meet the requirements of ISO 22716:2007.
  • SOP for Line clearance. Describes how line clearance is carried out and controlled to meet the requirements of ISO 22716:2007.
  • SOP for Equipment cleaning and sanitization. Describes how equipment cleaning and sanitization is carried out and controlled to meet the requirements of ISO 22716:2007.
  • SOP for General housekeeping. Describes how general housekeeping is carried out and controlled to meet the requirements of ISO 22716:2007.
  • SOP for Entry / Exit procedure - Personnel hygiene. Describes how entry / Exit procedure - Personnel hygiene is carried out and controlled to meet the requirements of ISO 22716:2007.
  • SOP for Floor cleaning. Describes how floor cleaning is carried out and controlled to meet the requirements of ISO 22716:2007.
  • SOP for Cleaning of doors, Windows, Walls and tube light and fan. Describes how cleaning of doors, Windows, Walls and tube light and fan is carried out and controlled to meet the requirements of ISO 22716:2007.
  • SOP for Incident reporting. Describes how incident reporting is carried out and controlled to meet the requirements of ISO 22716:2007.
FORMS Forms and records (42)
  • Purchase order. A standard order form that states your requirements to suppliers clearly.
  • Indent cum Incoming inspection report. Form used to record indent cum Incoming inspection report as evidence for the management system.
  • Approved Vendor list cum open purchase order. Form used to record approved Vendor list cum open purchase order as evidence for the management system.
  • Supplier Registration form. Collects supplier details and capability information for evaluation.
  • Open purchase order. Form used to record open purchase order as evidence for the management system.
  • Daily stock statement. Records daily stock levels for control and traceability.
  • Gate pass. Controls and records the movement of goods in and out of the site.
  • Breakdown history card. Records equipment breakdowns and repairs over time.
  • Preventive maintenance schedule. Plans routine maintenance to keep equipment fit for use.
  • Equipment Wise preventive maintenance checkpoints. Form used to record equipment Wise preventive maintenance checkpoints as evidence for the management system.
  • Daily pm check point. Form used to record daily pm check point as evidence for the management system.
  • PM Checkpoints for Building & civil work. Form used to record pM Checkpoints for Building & civil work as evidence for the management system.
  • Order form/ confirmation. Form used to record order form/ confirmation as evidence for the management system.
  • Customer Complaint report. Captures a customer complaint, the investigation, and how it was resolved.
  • Customer feedback form. Collects customer satisfaction data to feed monitoring and improvement.
  • Customer property monitoring register. Form used to record customer property monitoring register as evidence for the management system.
  • Master list cum distribution list of documents. Form used to record master list cum distribution list of documents as evidence for the management system.
  • Change note. Form used to record change note as evidence for the management system.
  • Calibration status of instrument / equipment. Form used to record calibration status of instrument / equipment as evidence for the management system.
  • Master list of records. An index of all quality records, showing where each is stored and how long it is kept.
  • Quality objective monitoring report. Form used to record quality objective monitoring report as evidence for the management system.
  • Audit plan / schedule. Form used to record audit plan / schedule as evidence for the management system.
  • Internal Audit Non-Conformity Report. Form used to record internal Audit Non-Conformity Report as evidence for the management system.
  • Clause-wise Document-wise Audit Review Report. Form used to record clause-wise Document-wise Audit Review Report as evidence for the management system.
  • Continual Improvement Plan. Form used to record continual Improvement Plan as evidence for the management system.
  • Corrective Action Report. Logs a nonconformity, its root cause, the action taken, and the check that it worked.
  • Preventive Action Report. Form used to record preventive Action Report as evidence for the management system.
  • Qualitative Process Monitoring Report. Form used to record qualitative Process Monitoring Report as evidence for the management system.
  • Vendor Rating. Form used to record vendor Rating as evidence for the management system.
  • List of license/certificate. Form used to record list of license/certificate as evidence for the management system.
  • Training Calendar. Form used to record training Calendar as evidence for the management system.
  • Training Need Cum Records Sheet. Form used to record training Need Cum Records Sheet as evidence for the management system.
  • Induction Training Report. Form used to record induction Training Report as evidence for the management system.
  • Job Description and Specification. Form used to record job Description and Specification as evidence for the management system.
  • Skill Matrix. Form used to record skill Matrix as evidence for the management system.
  • Training Report. Form used to record training Report as evidence for the management system.
  • Skill Matrix for QC Personnel. Form used to record skill Matrix for QC Personnel as evidence for the management system.
  • Housekeeping record. Form used to record housekeeping record as evidence for the management system.
  • Visitor gate pass. Form used to record visitor gate pass as evidence for the management system.
  • Incident Reporting form. Form used to record incident Reporting form as evidence for the management system.
  • Rodent trapping record. Form used to record rodent trapping record as evidence for the management system.
  • Sanitation report. Form used to record sanitation report as evidence for the management system.
What you gain

Why teams choose a ready-made kit

Save months of work

The writing is done. You edit instead of authoring from a blank page.

Avoid consultant fees

Get a professional system for a fraction of the cost of hiring one.

Nothing missed

Mapped clause by clause so every requirement is covered.

Written in plain English

Easy to read, easy to adapt, no jargon you have to decode.

Audit-ready evidence

Forms and registers capture exactly what an auditor asks to see.

Yours to keep

A perpetual licence for your whole team, with free updates.

How to use it

From download to audit ready in five steps

Download

The full set arrives by email in minutes, in Word and Excel.

Customise

Swap the highlighted placeholders for your own company details.

Implement

Roll out the procedures and capture evidence on the forms.

Audit and review

Use the internal audit checklist and management review templates.

Get certified

Face the auditor with a complete, consistent system.

Who it is for

Built for the people who have to get it done

  • Companies going for ISO 22716:2007 certification for the first time.
  • Quality and compliance managers who want a proven framework, not a blank page.
  • Businesses asked for a documented system for a tender, a client, or pre-qualification.
  • Consultants and trainers who need an editable base to adapt for clients.
How it is delivered

Secure, editable, and yours to keep

📥

24-hour delivery

Files sent securely within 24 working hours of payment.

✍️

Fully editable

Microsoft Word and Excel, with placeholders to fill in.

♾️

Free updates

If the standard is revised, you get the update free.

👥

Team licence

One organisation, unlimited internal users, perpetual.

Compare the options

Kit, consultant, or from scratch

What mattersFrom scratchHire a consultantisofolder kit
Time to a full document setMonthsWeeksThe same day
Typical costYour timeThousands$149 once
Written by expertsNoYesYes
Mapped to every clauseRiskyUsuallyYes
You keep full controlYesLimitedYes, fully editable
Free updates on revisionNoExtra feeIncluded
Our experience

Documentation is all we do, and we have done it since 2017

isofolder is a team of auditing and consulting professionals with more than 80 years of combined experience. Our kits are written by practitioners and reviewed by working auditors, then refined across many real certification projects. When you buy from us, you are buying a system that has already helped companies pass their audits.

If you ever need a document that is specific to your operation and not already in the kit, our team will prepare it for you.

2017Trading since
2,000+Products delivered
750+Projects completed
100+Standards covered
What buyers say

Trusted by teams getting certified

★★★★★

The documents were well structured and easy to adapt. We cleared our certification audit with no major findings.

Quality ManagerManufacturing, United Kingdom
★★★★★

Saved us weeks of writing. Everything was mapped to the clauses, so we knew nothing was missing.

Operations LeadFood business, UAE
★★★★★

Clear, professional and fully editable. Far better value than the consultant quotes we received.

FounderServices company, United States
See it first

Not sure yet? Look inside before you buy

Download a free sample document from the ISO 22716:2007 toolkit and judge the quality and writing style for yourself. No risk, no obligation.

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Questions

ISO 22716:2007 toolkit, frequently asked

What does the ISO 22716:2007 toolkit include?+
A clause-by-clause ISO 22716:2007 manual, 38 procedures, and 42 ready-to-use forms and records, plus sample filled examples. Everything is editable in Microsoft Word and Excel, and the full list is shown on this page.
Will it help me pass a certification audit?+
Yes. The documents are structured to the ISO 22716:2007 clauses an auditor checks and are written by experienced practitioners. You customise and implement them, and the kit gives you a complete, auditor ready system as your foundation.
What formats do I get, and can I edit them?+
Everything comes in editable Microsoft Word and Excel, with any presentations in PowerPoint. You replace the highlighted placeholders with your own details. No special software is needed.
How long does it take to customise?+
Most organisations tailor the core documents within a few days rather than the weeks or months it takes to write from a blank page. The manual and procedures are already written, so you are editing, not authoring.
How is it delivered?+
After your payment is confirmed, we send your files to you securely within 24 working hours, and usually much sooner. To keep the documents safe, we do not store them on public-facing servers.
Is there a licence limit or a subscription?+
There is no subscription. One purchase gives your organisation a perpetual licence with unlimited internal users, so your whole team can work on the documents.
Do I get updates when the standard changes?+
If ISO 22716:2007 is revised, you receive the updated documents free of charge, so your system stays current without buying again.
Is it suitable for my industry?+
The kit is written to the ISO 22716:2007 requirements, which apply across sectors. The documents are editable, so you keep what fits your operation and adapt or set aside anything that does not. It has been used by manufacturers, food businesses, laboratories, healthcare, IT and service companies.
How is this different from free templates online?+
Free templates are usually incomplete, generic, or out of date, and they leave you guessing what an auditor expects. This kit is a complete, current, clause-mapped set written by practitioners, with every document listed and explained so there are no surprises.
Can I check the toolkit before I buy?+
Yes. You can download a free sample document first to check the quality and writing style, so you can decide with confidence.
Complete your system

Frequently bought together

Get your ISO 22716:2007 system, ready today

Download the complete, editable toolkit and start building an audit ready system in minutes, with a free sample available before you buy.

ISO 22716:2007 Documentation Toolkit 81 documents, Word and Excel, delivery within 24 working hours $149