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ISO/IEC 17020:2012 Package

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ISO/IEC 17020:2012
ISO/IEC 17020:2012 Package

ISO/IEC 17020 2012 complete package

2012 version

ISO/IEC 17020:2012 Package
ISO/IEC 17020:2012 Package
ISO/IEC 17020:2012 Package
All you need to achieve ISO/IEC 17020 Accreditation
1 hour 1-to-1 Online Sessions with our ISO Expert
Continuous Email Support and Updates

 Price :  389 $

Play Video about ISOIEC 17020 2012 Documentation Package

The complete ISO/IEC 17020:2012 package is a comprehensive document package that contains everything from templates of procedures, processes, forms, checklists, tools, detailed guides, and instructions needed to:

  • Start your ISO/IEC 17020 process.
  • Create your ISO/IEC 17020 documentation.
  • Quickly achieve ISO/IEC 17020 accreditation.
  • Benefit from an ISO/IEC 17020 management system that is simple and adapted to the needs of your inspection body.
ISO/IEC 17020:2012 Package
Save time

Why start with a blank page. Start your Project TODAY, and save up to 80% on your time and money.

ISO/IEC 17020:2012 Package
Online consulting

 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.

ISO/IEC 17020:2012 Package
Save money

Cost-Effective Implementation: Much cheaper than an on-site consultant, and requires much less time than doing it from scratch

ISO/IEC 17020 2012 Version Complete Package

Added Value: All ISO/IEC 17020:2012 requirements have been developed into an efficient process that adds operational value to your inspection body and consequently increases productivity.

Effective: Minimal effort is required to follow the procedures necessary to meet all requirements of ISO/IEC 17020.

Simplified: Bureaucracy and excessive paperwork have been eliminated from each process to make it easy—while remaining fully compliant with ISO/IEC 17020:2012.

 

Start your Project TODAY, and save up to 80% on your time and money.

 

The all-in-one document package for ISO/IEC 17020 2012 version

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

     

ISO/IEC 17020:2012 Package

Procedures:

  • Competence and Training Procedure
  • Complaints Handling Procedure
  • Confidentiality and Data Protection Procedure
  • Confidentiality and Impartiality Procedure
  • Contract Review Procedure
  • Control of Documents Procedure
  • Control of Nonconforming Services Procedure
  • Control of Records Procedure
  • Corrective Action Procedure
  • Equipment Calibration and Maintenance Procedure
  • Inspection Planning and Execution Procedure
  • Internal Audit Procedure
  • Management Review Procedure
  • Preventive Action Procedure
  • Purchasing and Supplier Evaluation Procedure
  • Risk Management Procedure
ISO/IEC 17020:2012 Package

Inspection Schemes

  • Emissions Inspection Scheme
  • Environmental Compliance Inspection Scheme
  • Fleet Maintenance and Safety Inspection Scheme
  • Pre-Shipment and Post-Delivery Inspection Scheme
  • Safety Compliance Inspection Scheme
ISO/IEC 17020:2012 Package

Manual and quality policy

  • ISO/IEC 17020 2012 Quality Manual
ISO/IEC 17020:2012 Package

Forms

  • Client Feedback Form
  • Complaint and Appeal Form
  • Confidentiality Agreement Form
  • Corrective Action Request
  • Document Change Request Form
  • Document Control Form
  • Equipment Calibration and Maintenance Record
  • Equipment Verification and Check Form
  • Impartiality Risk Assessment Form
  • Inspection Checklist Form
  • Inspection Report
  • Inspection Scheduling and Planning Form
  • Inspector Competency Assessment Form
  • Internal Audit Checklist
  • Management Review Form
  • Nonconformity Report
  • Risk Assessment and Mitigation Form
  • Training Record Form
  • Training Needs Analysis Form
  • Corrective and Preventive Action
ISO/IEC 17020:2012 Package

Comprehensive Guide to ISO/IEC 17020:2012: Chapter-by-Chapter Breakdown of Inspection Body Requirements

Chapter 1: Scope

This chapter defines the scope of ISO/IEC 17020:2012 and its applicability to organizations conducting inspections.

Key Requirements:
  • Applicability: ISO 17020 applies to organizations that perform inspections of products, processes, services, or installations. The standard ensures that inspection bodies operate competently and impartially to deliver reliable inspection results.
  • Inspection Activities: The scope covers different types of inspections, including first-party, second-party, and third-party inspections, ensuring that all categories meet consistent standards for quality and integrity.

Chapter 2: Normative References

This chapter lists the normative references that are essential for implementing ISO/IEC 17020:2012.

Key Requirements:
  • Referenced Standards: This standard refers to other ISO and IEC documents that provide additional guidelines for inspection bodies, ensuring compatibility and alignment with international best practices.

Change in structure :

ISO 17020

Chapter 3: Terms and Definitions

This chapter provides definitions for key terms used throughout ISO 17020 to ensure consistent understanding and application of the standard’s requirements.

Key Requirements:
  • Key Terminology: Definitions include terms like “inspection,” “inspection body,” “impartiality,” and “inspection report.” Understanding these terms is crucial for correct interpretation and application of the standard.

Chapter 4: General Requirements

This chapter covers the overall principles that inspection bodies must adhere to, focusing on impartiality, independence, and confidentiality.

Key Requirements:
  • Impartiality: Inspection bodies must maintain impartiality in their activities, ensuring that inspection results are free from any conflicts of interest. Mechanisms should be in place to manage any risks to impartiality.
  • Independence: The level of independence of the inspection body should correspond to its type (A, B, or C), with Type A being the most independent from any other activities that might influence inspection results.
  • Confidentiality: Inspection bodies must establish procedures to protect confidential information obtained during inspection activities. This ensures the privacy of client data and inspection results.

Chapter 5: Structural Requirements

This chapter details the organizational structure required for inspection bodies to ensure competence and impartiality.

Key Requirements:
  • Organizational Structure: Inspection bodies must have a clearly defined structure with established roles and responsibilities that support independence and impartial decision-making.
  • Separation of Activities: The structure should ensure that staff performing inspections are not influenced by other activities of the organization, such as design, production, or consulting, that could impact impartiality.

Chapter 6: Resource Requirements

This chapter outlines the personnel and infrastructure requirements for inspection bodies to conduct reliable and competent inspections.

Key Requirements:
  • Competence of Personnel: Inspection bodies must ensure that inspectors have the required knowledge, skills, and experience for the specific types of inspections they perform. Ongoing training must be provided to keep personnel up to date with new regulations and standards.
  • Infrastructure and Equipment: Adequate resources, including physical infrastructure and calibrated equipment, must be available to support inspection activities. Inspection bodies must maintain and calibrate equipment regularly to ensure accurate results.
  • Subcontracting: When an inspection body subcontracts any part of the inspection work, it must ensure that the subcontractor meets the same competence and impartiality requirements as the inspection body itself.

Chapter 7: Process Requirements

This chapter focuses on the operational processes involved in the planning, execution, and reporting of inspection activities.

Key Requirements:
  • Inspection Methods and Procedures: Inspection bodies must use appropriate methods and procedures that are documented and regularly reviewed. This ensures inspections are performed consistently and meet customer and regulatory requirements.
  • Handling of Inspection Items: Proper procedures must be in place to handle inspection items, ensuring they are protected and treated according to client requirements. This includes ensuring that test items are not contaminated or altered during inspection.
  • Reporting: Inspection bodies must provide clear, concise, and accurate inspection reports to clients. The report should include all necessary information, including the inspection results, methodologies used, and any deviations from standard procedures.
  • Management of Nonconforming Work: If inspection work is found to be nonconforming, the inspection body must take appropriate corrective actions. This includes investigating the root cause and implementing preventive measures to avoid recurrence.

Chapter 8: Management System Requirements

This chapter specifies the management system that inspection bodies must implement to ensure continuous improvement and consistent quality in their inspection activities.

Key Requirements:
  • Management System Options: Inspection bodies can implement a management system based on ISO 9001 or establish a system that fulfills the specific requirements of ISO 17020. The management system should support the consistent and effective delivery of inspection services.
  • Internal Audits: Inspection bodies must conduct regular internal audits to assess compliance with ISO 17020 and identify areas for improvement. The results of these audits should be documented and used to improve the effectiveness of the inspection body’s operations.
  • Corrective Actions: Nonconformities found during audits or other activities must be addressed through corrective actions, including root cause analysis and follow-up measures to ensure that issues are resolved.
  • Management Review: Top management must periodically review the management system to ensure its continuing suitability, adequacy, and effectiveness. This includes reviewing audit results, customer feedback, and the performance of inspection activities.
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If for whatever reason during the FIRST 30 days of your purchase, you are not satisfied for any reason, simply contact support@qse-academy.com and our support team will issue you an immediate and full refund.

All documents required for the implementation of ISO/IEC 17020 2012

The package includes all the documents you need to comply with ISO/IEC 17020 2012 – these documents are fully acceptable by the accreditation audit.

ISO/IEC 17020:2012 Package
Fully editable documents

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.

ISO/IEC 17020:2012
Documents are 90% complete and require only a simple customization

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.

We presented the ISO 17020 documentation, so as to assure all its users that they have completed everything accurately and with the utmost efficiency.

ISO/IEC 17020:2012 Package
Clearly organized, understandable steps

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 17020 2012 Kit

Price: 389 $
– Documentation included: 58 documents for the implementation of ISO 17020
– Language: English
– Documents are fully editable – just enter the information specific to your business.
– Acceptable for the ISO 17020 2012 accreditation audit? Yes, all the documents required by ISO 17020 2012 are included, as well as the quality policy and 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 17020:2012
ISO/IEC 17020:2012 Package

Complete ISO/IEC 17020 2012 Package

The complete kit to implement ISO/IEC 17020

Price :  389 $

ISO/IEC 17020 Implementation Project Plan

Achieving ISO 17020 is a significant milestone for any organization, signifying a commitment to data protection and privacy. Our expert consultants are here to guide you through every step of the implementation process, from initial consultation and gap analysis to final assessment and compliance certification. With our comprehensive project plan, tailored training programs, and dedicated support, we ensure your organization meets all ISO 17020 requirements efficiently and effectively. Partner with us to enhance your organization’s credibility, improve data handling processes, and gain trust on an international scale. Let us help you achieve excellence in data privacy management.

Introduction: Project Kick-off and Gap Analysis 

Introductory Tasks

1.1 ISO 17020 Kick-off and Awareness

Task: Organize Kick-off Meeting

  • Description: Conduct a kick-off meeting to introduce the ISO/IEC 17020:2012 project to key stakeholders. Discuss objectives, timelines, scope, and responsibilities.
  • Deliverables: Project plan, meeting agenda, and minutes.
  • Meeting: Initial consultation with senior management, technical staff, and the implementation team.

1.2 Perform Gap Analysis

Task: Conduct Gap Analysis Against ISO/IEC 17020:2012 Requirements

  • Description: Assess current inspection processes, management systems, and technical operations against ISO/IEC 17020:2012 requirements to identify gaps.
  • Deliverables: Gap analysis report with identified non-conformities.
  • Meeting: Present findings to senior management and the technical team.

Section 1: Quality Management System (QMS) Documentation and Policy Development 

2.1 Develop and Document Quality Policy and Objectives (ISO 17020 Clause 8.1)

Task: Define Quality Policy and Objectives

  • Description: Develop the organization’s quality policy and measurable objectives, ensuring alignment with ISO/IEC 17020:2012 requirements.
  • Deliverables: Quality policy and objectives document.
  • Meeting: Review and approve the policy with senior management.

2.2 Develop Quality Management System (QMS) Documentation

Task: Create QMS Documentation (Manual, Procedures, Work Instructions)

  • Description: Develop necessary documentation for the QMS, including a quality manual, process procedures, and work instructions that cover all key areas of inspection activities.
  • Deliverables: Quality manual, procedures, work instructions.
  • Meeting: Review QMS documentation with the quality and technical teams.

Section 2: Impartiality, Independence, and Confidentiality 

3.1 Establish Policies for Impartiality and Independence (ISO 17020 Clause 4.1)

Task: Develop Impartiality and Independence Policy

  • Description: Create policies to ensure that the organization’s inspection activities are carried out impartially, without any conflicts of interest, and that independence is maintained.
  • Deliverables: Impartiality and independence policy.
  • Meeting: Review policy with senior management, inspection staff, and key stakeholders.

3.2 Develop Confidentiality Procedures (ISO 17020 Clause 4.2)

Task: Implement Confidentiality and Data Protection Measures

  • Description: Establish procedures to protect the confidentiality of client information and inspection results, ensuring all personnel are aware of their responsibilities.
  • Deliverables: Confidentiality procedures, non-disclosure agreements (NDAs).
  • Meeting: Train staff on confidentiality procedures and responsibilities.

Section 3: Competence of Personnel and Inspection Methods  

4.1 Ensure Competence of Inspection Personnel (ISO 17020 Clause 6.1)

Task: Define Competence Requirements for Inspection Personnel

  • Description: Establish criteria for the competence of inspection personnel, including qualifications, skills, experience, and training required for each role.
  • Deliverables: Competence matrix, job descriptions, and training plans.
  • Meeting: Review competence criteria with HR and department heads.

4.2 Develop Inspection Methods and Procedures (ISO 17020 Clause 7.1)

Task: Document and Implement Inspection Procedures

  • Description: Develop standardized procedures for conducting inspections, ensuring all methods are validated, consistently applied, and documented.
  • Deliverables: Inspection methods and procedures.
  • Meeting: Review inspection procedures with technical teams and conduct training sessions.

Section 4: Control of Documents and Records 

5.1 Implement Document Control System (ISO 17020 Clause 8.3)

Task: Establish Procedures for Document Control

  • Description: Implement a document control system to ensure all QMS-related documents, procedures, and inspection records are managed, reviewed, and updated as required.
  • Deliverables: Document control procedures and document register.
  • Meeting: Train staff on the document control system.

5.2 Implement Record Keeping and Traceability (ISO 17020 Clause 8.4)

Task: Establish Record Control Procedures

  • Description: Develop procedures to manage and retain records of inspection activities, ensuring traceability and the secure storage of records.
  • Deliverables: Record control procedures, record retention schedules.
  • Meeting: Review procedures with the quality team and train staff on record management.

Section 5: Corrective Actions and Non-Conformity Management 

6.1 Implement Non-Conformity and Corrective Action Procedures (ISO 17020 Clause 8.7)

Task: Establish Procedures for Handling Non-Conformities

  • Description: Develop a process for identifying, documenting, and addressing non-conformities in inspection activities, including the root cause analysis and corrective actions.
  • Deliverables: Non-conformance reports, corrective action plans.
  • Meeting: Review non-conformity handling with management and inspection staff.

6.2 Implement Continual Improvement Processes (ISO 17020 Clause 8.6)

Task: Establish Process for Continuous Improvement

  • Description: Develop processes to review and improve inspection activities regularly, using performance data, audit results, and feedback to drive improvements.
  • Deliverables: Improvement plans, feedback mechanisms.
  • Meeting: Review improvement initiatives with senior management and inspection teams.

Section 6: Internal Audits and Management Review 

7.1 Develop Internal Audit Program (ISO 17020 Clause 8.6)

Task: Create Internal Audit Plan

  • Description: Establish an internal audit program to regularly assess the effectiveness of the QMS and compliance with ISO/IEC 17020 requirements, identifying areas for improvement.
  • Deliverables: Internal audit plan, audit schedule, and checklist.
  • Meeting: Review audit plan with the internal audit team and senior management.

7.2 Conduct Internal Audits

Task: Perform Internal Audits

  • Description: Conduct internal audits to verify compliance with the QMS, inspection procedures, and ISO/IEC 17020 requirements. Identify non-conformities and areas for improvement.
  • Deliverables: Internal audit reports, non-conformance reports.
  • Meeting: Post-audit review meeting to discuss findings and corrective actions.

7.3 Conduct Management Review (ISO 17020 Clause 8.5)

Task: Perform Management Review of QMS and Inspection Activities

  • Description: Conduct a management review to evaluate the performance of the QMS and inspection processes, assess opportunities for improvement, and ensure compliance with ISO/IEC 17020.
  • Deliverables: Management review meeting minutes, action plans.
  • Meeting: Present review findings and improvement plans to senior management.

Final Assessment: Certification Preparation and External Audit 

8.1 Conduct Pre-Certification Internal Audit

Task: Perform Pre-Certification Internal Audit

  • Description: Conduct a final internal audit to ensure that the QMS and inspection activities meet ISO/IEC 17020:2012 requirements and are ready for the certification audit. Address any remaining non-conformities.
  • Deliverables: Pre-certification audit report, corrective action plans.
  • Meeting: Final review meeting with senior management and the quality team.

8.2 Certification Body Selection and External Audit

Task: Select Certification Body and Schedule Certification Audit

  • Description: Research and select an accredited certification body for ISO/IEC 17020. Schedule the external audit and ensure the organization is fully prepared.
  • Deliverables: Certification body selection report, external audit schedule.
  • Meeting: Final meeting with management and inspection team to confirm readiness for certification.

This 8-month project plan for ISO/IEC 17020:2012 implementation ensures a structured approach to achieving accreditation for inspection bodies. It covers key areas such as impartiality, competence, non-conformance management, internal audits, and certification preparation, aligning the organization with ISO/IEC 17020 requirements for inspection activities.

What our customers think:

ISO/IEC 17020:2012 Package

We needed the ISO/IEC 17020:2012 package from QSE Academy to expedite this whole accreditation routine for our team. The docs were very comprehensive, but simple enough for us to customize everything quickly. The templates were formatted nicely and easy to customize for our type of inspections. The one-to-one with their expert was great to consolidate some technical info as well. This package is what led us to our accreditation. I can recommend the toolkit for any inspection body that searches a cost-effective way to collect real pressure data.

James Anderson

Head of Operations

ISO/IEC 17020:2012 Package
ISO/IEC 17020:2012 Package

QSE Academy provided an excellent ISO/IEC 17020:2012 package. The documentation was sufficient and satisfied all the needs required to gain an accreditation. We were to move quickly with the aid of customizable templates, and received excellent support. The consulting session were of great help, we gained a lot of insights and having email assistance as an ongoing support has been tremendously helpful. The package was well worth the money for our organization, and it’s something we would highly recommend.

Sarah Mitchell

Compliance Officer

ISO/IEC 17020:2012 Package

Frequently Asked Questions

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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.

When you make a purchase, you will be contacted by an account manager who will assist you throughout the process. Our scheduling is flexible to accommodate your needs. Upon requesting a meeting, you will receive a link to select a time that works best for you. Additionally, you can communicate with the ISO expert via email.

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ISOIEC 17020 Implementation Project Plan

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Kickstart your accreditation with a step-by-step project plan. Streamline the process, save time, and achieve compliance with ease

 

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