ISO/IEC 17021-1:2015 Package
2025-03-14 16:06ISO/IEC 17021-1:2015 Package
ISO/IEC 17021-1 Documentation Package
2015 version
- Achieve the highest international accreditation standard for certification bodies.
- ➡️ All documents required for accreditation.
- ➡️ 30-day money-back guarantee.
- ➡️ Immediate download
- ➡️ Support available 7 days a week
Price : 589 $
Accreditation Made Simple and Accessible for Your Business
If you’re running a certification body, chances are you’re always looking for ways to improve your processes and demonstrate compliance with international standards.
That’s where the ISO/IEC 17021-1 Documentation Package comes in.
This package includes all the essential documents you need to achieve ISO/IEC 17021-1 certification, the international standard that sets requirements for bodies providing audit and certification of management systems.
So why wait? Get started today and take the next step toward ISO/IEC 17021-1 certification!
Why start with a blank page. Start your Project TODAY, and save up to 80% on your time and money.
This package comes with 1 hour Live 1-to-1 Online Session with ISO consultant, document reviews, continual email support for 12 months and regular update service.
Cost-Effective Implementation: Much cheaper than an on-site consultant, and requires much less time than doing it from scratch
👉 What is ISO/IEC 17021-1:2015?
ISO/IEC 17021-1:2015 is an international standard that sets requirements for certification bodies conducting audits and certifying management systems. It ensures that certification activities are consistent, impartial, and credible while increasing customer confidence in certified products and services.
Key Objectives of the Standard:
- Establish a reliable certification framework for management systems.
- Ensure consistency, impartiality, and competence in certification bodies.
- Improve customer trust in certified organizations.
- Outline requirements for audit processes, documentation, and management system oversight.
What Does the Standard Cover?
🔹 Principles of Certification Activities
- Defines the core requirements certification bodies must follow.
- Ensures transparency, integrity, and objectivity in certification decisions.
🔹 Management System Requirements
- Certification bodies must implement a structured management system.
- Requires clear documentation of processes and procedures.
- Emphasizes the importance of handling confidentiality, complaints, and appeals.
🔹 Audit Process Requirements
- Outlines steps for planning and conducting audits.
- Establishes methods for gathering and evaluating audit evidence.
- Ensures that certification decisions are based on verified, objective evidence.
Why is ISO/IEC 17021-1:2015 Important?
✅ Ensures certification bodies operate competently and impartially.
✅ Strengthens customer trust in certified organizations.
✅ Helps businesses maintain a competitive edge through internationally recognized certification.
✅ Improves audit reliability by requiring skilled, knowledgeable, and impartial auditors.
ISO/IEC 17021-1:2015 is the foundation for credible and effective certification bodies. Implementing this standard ensures compliance with international requirements and enhances the value of certifications in the global market.
The all-in-one package for ISO/IEC 17021-1 Documentation
Save time, save money and simplify the accreditation process.
Documents included:
👉 This package provides you with the following features:
- Full lifetime access
- Access on a laptop, desktop, and mobile
Procedures
- Human Resources Management Procedure
- Contract Review Procedure
- Purchasing and Subcontracting Procedure
- Certification Process Procedure
- Change Management Procedure
- Legal Compliance Procedure
- Logo and Certification Mark Usage Procedure
- Document and Records Control Procedure
- Internal Audit Procedure
- Management Review Procedure
- Corrective Action Procedure
- Complaints and Appeals Handling Procedure
- Audit Conducting Procedure
- Mandays Estimation Procedure
- Impartiality Management Procedure
Quality Manual
- ISO/IEC 17021 Quality Manual (55 Pages)
- ISO/IEC 17021 Implementation Checklist
Certification Schemes:
- ISO 9001:2015 Quality Management System Certification Scheme (QMS)
- ISO 14001:2015 Environmental Management System Certification Scheme (EMS)
- ISO 45001:2018 Occupational Health and Safety Management System Certification Scheme (OHSMS)
- ISO 22000:2018 Food Safety Management System Certification Scheme (FSMS)
- ISO 27001:2022 Information Security Management System Certification Scheme (ISMS)
Records and Forms:
- Application for Certification Form
- Contract Review Form
- Certification Agreement Form
- Audit Plan Template
- Audit Report Form
- Nonconformity Report Form
- Corrective Action Request Form
- Audit Checklist Template
- Auditor Competence Evaluation Form
- Audit Program Form
- Stage 1 Audit Report Form
- Stage 2 Audit Report Form
- Certification Decision Report
- Surveillance Audit Report Form
- Re-Certification Audit Report Form
- Impartiality and Conflict of Interest Declaration
- Appeals and Complaints Log
- Management Review Meeting Minutes Form
- Internal Audit Report Form
- Impartiality Risk Assessment Form
- Certification Scope Statement Form
- Certificate Issuance Approval Form
- Suspension and Withdrawal Decision Form
- Use of Certification Mark Agreement
- Witnessed Audit Report Form
- Confidentiality Agreement Form
- Record Retention and Control Form
- Corrective Action Effectiveness Verification Form
- Personnel Training and Competence Record
- Client Satisfaction Survey Form
ISO/IEC 17021-1 Documentation Requirements Explained
The ISO/IEC 17021-1 Documentation Package is essential for certification bodies (CBs) that conduct audits and certify management systems. This package includes all the necessary documentation to help your organization comply with ISO/IEC 17021-1:2015, the international standard that sets competence, consistency, and impartiality requirements for management system certification bodies.
Comprehensive and well-structured documentation is key to ensuring a transparent, systematic, and internationally recognized certification process. From audit procedures to certification decisions, having robust documentation ensures smooth operations, regulatory compliance, and accreditation success.
Why ISO/IEC 17021-1 Documentation Matters
Proper documentation plays a crucial role in maintaining the integrity and efficiency of your certification body. It serves as a structured roadmap for conducting management system audits, making informed certification decisions, and demonstrating compliance with international accreditation requirements.
This package includes:
Key ISO/IEC 17021-1 Documentation Categories
| Document | Purpose in Certification Process |
|---|---|
| Certification Agreement | Defines terms and responsibilities between CB and clients |
| Application Documents | Initiates and formalizes the certification request |
| Audit Procedures | Details standardized steps for conducting management system audits |
| Competence and Training Records | Maintains staff qualification, training, and ongoing professional development |
| Audit Reports | Records findings and observations from certification audits |
| Non-Conformity Reports | Highlights deviations and required corrective actions |
| Certification Decisions | Documents the outcome of the assessment process |
Core ISO/IEC 17021-1 Documentation Requirements
Management System Documentation
To comply with ISO/IEC 17021-1:2015, certification bodies must maintain a structured management system, ensuring impartiality, competence, and quality-driven decision-making. Essential documents include:
- Quality Manual – Outlines the CB’s management system, scope, and operational policies.
- Policies & Standard Operating Procedures (SOPs) – Define key activities, from audit planning to certification issuance.
- Risk Management Procedures – Ensure consistent identification and management of risks related to impartiality and conflicts of interest.
- Impartiality Documentation – Provides evidence of the CB’s impartiality in decision-making and certification processes.
Audit Process Documentation
Well-documented audit processes ensure transparency, consistency, and traceability. This package includes:
- Audit Planning Documents – Templates for audit scope, objectives, and scheduling.
- Audit Checklists – Standardized checklists to guide auditors through the evaluation process.
- Corrective Action Procedures – Guidelines for addressing and resolving non-conformities.
- Surveillance and Recertification Procedures – Ensures ongoing compliance and periodic re-evaluation of certified organizations.
Legal and Contractual Documentation
- Certification Agreements – Contracts outlining terms, conditions, and obligations between the CB and clients.
- Confidentiality & Impartiality Declarations – Ensuring that auditors and certification body personnel remain neutral and unbiased.
- Liability & Insurance Documents – Providing proof of coverage for certification activities.
Surveillance and Recertification Documentation
ISO/IEC 17021-1:2015 requires certification bodies to maintain documentation for ongoing compliance and recertification. This includes:
- Surveillance Audit Reports – Records of periodic audits confirming continued adherence to the certified management system.
- Recertification Procedures – Clear guidelines on how organizations renew their certification.
- Change Management Documentation – Handling revisions to certification requirements and processes.
Ensure Compliance with ISO/IEC 17021-1:2015 Today!
Achieving ISO/IEC 17021-1:2015 certification can be complex, but with the ISO/IEC 17021-1:2015 Documentation Package, your certification body will have everything needed to streamline compliance and ensure internationally recognized certification processes.
💡 Get started today and take your certification body to the next level with a structured, compliant, and efficient management system!
30 Days Money Back
Guarantee
If for any reason you’re not completely satisfied within the first 30 days of your purchase, just email us at support@qse-academy.com, and we’ll provide you with a prompt, full refund—no questions asked.
The package includes all the documents you need to comply with ISO/IEC 17021 2015 – these documents are fully acceptable by the accreditation audit.
All documents are in MS Word or MS Excel, to make them very easy to customize for your business. You can customize them by adding company logos and colors, and edit headers and footers to match your favorite style.
We have already completed about 90% of the information requested on the documents. To complete them you must fill in only the name of the company, the responsible parties, and any other information unique to your company. you will be guided through the process, commenting on the elements that are needed and those that are optional.
All the documents are made so that you can follow the proposed order perfectly, which allows you to make sure that nothing is missing, and that no one gets lost in the process.
The included comments and flowcharts help your staff understand each document and its usefulness, which helps you to make quality management more fluid, and processes easier to follow.
Features of the complete ISO/IEC 17021-1 Documentation Kit
Price: 589 $
– Documentation included: 52 documents for the implementation of ISO 17021
– Language: English
– Documents are fully editable – just enter the information specific to your business.
– Acceptable for the ISO/IEC 17021 2015 accreditation audit? Yes, all the documents required by ISO/IEC 17021-1 2015 are included, as well as the current but optional procedures
Instant Delivery – The package is downloadable immediately after purchase
Free Consultation – In addition, you can submit two complete documents for review by professionals.
Created for your business – The models are optimized for small and medium businesses.
ISO/IEC 17021-1 Documentation Package
The comprehensive kit for ISO/IEC 17021-1 Documentation is designed to equip certification bodies with all the necessary tools to achieve accreditation under this standard.
Price : 589 $
What our customers think:
“We were struggling to put together a structured system for ISO/IEC 17021-1 certification, but this kit made everything so much easier. The documents are clear, well-organized, and covered exactly what we needed. It saved us months of work, and we passed our audit with confidence!”
Dubai, UAE – Ahmed R.
(Certification Manager)
“I was skeptical at first, but this documentation package exceeded my expectations. It covers everything from audit procedures to impartiality management. The templates are easy to customize, and it helped us streamline our processes significantly. Highly recommended for any certification body!”
Houston, USA – Jessica L.
(Quality Director)
Frequently Asked Questions
How long will it take to receive the complete package of documents after I place my order?
Upon completing your purchase, you will be redirected to the download page immediately. Additionally, a link to access your file will be sent to your email. The files are provided in a .zip format, which you will need to extract. If you encounter any issues with the download, please do not hesitate to contact us at support@qse-academy.com. Our support team is always ready to assist you.
What payment methods can I use?
We offer several payment options for your convenience. You can choose to pay using a credit card, debit card, or PayPal. Additionally, we provide a flexible layaway plan for those who prefer to pay for their purchase over time. If you have any questions about our payment options, please don’t hesitate to contact us.
Do you offer a money-back guarantee if I'm not satisfied with the service?
We offer a 30-day money-back guarantee. If you are not satisfied with our service for any reason, you can cancel within the first 30 days and receive a full refund, no questions asked.
Is there ongoing support or assistance available after my purchase?
Yes! At QSE Academy, our ISO experts provide continued support by answering your queries via email. You can expect a detailed response within 24 to 48 hours to help you move forward confidently.
Are updates to the documentation package included after purchase?
Absolutely. To ensure your documentation remains reliable and compliant, we update our packages every 6 months. Existing customers receive these minor updates at no extra charge. However, when there’s a major revision of the ISO standard itself, you’ll need to purchase an updated kit to align with the new standard.
Will I receive a valid invoice for my business expenses after completing the purchase?
Yes. After completing your purchase, you’ll immediately receive a valid invoice suitable for business and tax purposes. If you require any specific adjustments or details added to your invoice, please reach out to our support team.
Can I customize these documents for my company's specific needs?
Yes, the documents are fully customizable! You can easily edit, modify, and add your company’s logo to tailor them specifically for your organization. Additionally, if you’d prefer assistance, we offer a personalized “Done-For-You” customization service to deliver audit-ready documents tailored exactly to your organization’s requirements.
How quickly can I implement this ISO standard using your documentation?
Implementation time varies depending on your company’s engagement, resources, and experience. Typically, we’ve observed businesses successfully achieve compliance and certification within 3 to 6 months using our clear, structured documentation packages.
Do these documents guarantee successful certification?
While our documentation packages significantly simplify the certification process, the ultimate success of ISO certification depends on effective implementation. For organizations seeking further assurance, we also provide comprehensive support services, including guided implementation and internal audits, to help you confidently pass your certification audit.
Do you offer hands-on assistance if I need extra help during implementation?
Definitely! If you prefer a complete, hands-off solution, we offer a premium “Done-For-You” implementation service. Our ISO experts handle the full preparation, providing you with audit-ready documentation and detailed implementation support. You simply adopt the customized materials, follow the tailored guidelines, and confidently pass your audit.
