{"id":8081,"date":"2026-10-29T13:00:00","date_gmt":"2026-10-29T13:00:00","guid":{"rendered":"https:\/\/icompliance.eu\/iso-9001-2026-changes-prepare\/"},"modified":"2026-10-29T12:56:00","modified_gmt":"2026-10-29T12:56:00","slug":"iso-9001-2026-changes-prepare","status":"publish","type":"post","link":"https:\/\/icompliance.eu\/en\/iso-9001-2026-changes-prepare\/","title":{"rendered":"ISO 9001:2026: What Changes and How to Prepare"},"content":{"rendered":"<p>ISO 9001:2026, published on 16 September 2026, is the sixth edition of the international standard for quality management systems. It replaces the 2015 edition, including Amendment 1:2024, and opens a new adaptation period for certified organisations. Information about the publication and status of the standard is available on the <a href=\"https:\/\/www.iso.org\/standard\/9001\" target=\"_blank\" rel=\"noopener\">official ISO 9001:2026 page<\/a>.<\/p>\n<p>For organisations that already have a quality management system (QMS) in place, the starting point is their existing work. The revision retains the foundation of the standard and introduces targeted changes, with particular emphasis on leadership, quality culture, ethical behaviour and the distinction between risks and opportunities.<\/p>\n<p>The challenge lies in understanding which adjustments make sense for each organisation, integrating them into existing processes and demonstrating that they work in day-to-day operations. An effective transition should not, therefore, be limited to updating procedures: it must translate into decisions, behaviours and results that are consistent with the QMS.<\/p>\n<h2>What changes in ISO 9001:2026?<\/h2>\n<h3>1. Greater clarity in managing risks and opportunities<\/h3>\n<p>The new edition makes a more explicit distinction between actions to address risks and actions to address opportunities. This change is detailed in the <a href=\"https:\/\/www.dqsglobal.com\/en\/explore\/focus-area\/iso-9001-revision-at-a-glance\" target=\"_blank\" rel=\"noopener\">DQS analysis<\/a>.<\/p>\n<p>In practice, it is worth checking whether opportunities receive sufficient attention during planning. Identifying threats is common practice; recognising potential improvements and deciding how to pursue them requires equally careful analysis.<\/p>\n<p>For example, recurring customer requests for faster information may reveal an opportunity to improve service follow-up. The organisation can assess the expected benefit, define an action, assign responsibilities and monitor the results.<\/p>\n<p>One practical recommendation is to make the distinction between risks and opportunities clear in the tools already in use. This distinction does not, in itself, require two separate registers. What matters is that the chosen method makes it possible to understand the assessment carried out, the decisions made and how the organisation monitors the effectiveness of its actions.<\/p>\n<h3>2. More explicit quality culture and ethical behaviour<\/h3>\n<p>The revision strengthens the role of top management in promoting a quality culture and ethical behaviour. It also reinforces people\u2019s awareness of these matters, according to the description of the changes provided by <a href=\"https:\/\/www.iso.org\/standard\/9001\" target=\"_blank\" rel=\"noopener\">ISO<\/a>.<\/p>\n<p>To prepare the organisation, start with specific situations: how are errors communicated? How is a complaint handled? What happens when a commercial deadline conflicts with quality criteria? Do people feel able to report a problem before it affects the customer?<\/p>\n<p>The answers help determine whether practices are consistent with the commitments made. Team meetings, training, management decisions, problem handling and internal communication can provide evidence of this consistency. Rather than creating formal statements, the priority is to ensure that day-to-day decisions reflect the culture the organisation intends to promote.<\/p>\n<h3>3. A clearer link between quality and strategy<\/h3>\n<p>The quality policy now has a more explicit link to the organisation\u2019s context and strategic direction. The revision therefore strengthens the role of the QMS in supporting business objectives, according to the information provided by <a href=\"https:\/\/www.iso.org\/standard\/9001\" target=\"_blank\" rel=\"noopener\">ISO<\/a>.<\/p>\n<p>A useful way to assess this alignment is to compare strategic priorities with quality objectives and indicators. If the organisation aims to grow in a more demanding market, for example, it may be necessary to review competencies, responsiveness, supplier control or customer satisfaction monitoring.<\/p>\n<p>The practical question is simple: do the quality objectives help achieve the organisation\u2019s priorities? If the connection is unclear, it may be necessary to review the objectives, the indicators used or how QMS results are considered in management decisions.<\/p>\n<h3>4. Context and climate change: reviewing what is relevant<\/h3>\n<p>Climate change had already been introduced into ISO 9001 through Amendment 1:2024. Its consideration should therefore not be presented as an exclusive new feature of the 2026 edition. The <a href=\"https:\/\/committee.iso.org\/files\/live\/sites\/tc176\/files\/PDF%20APG%20New%20Disclaimer%2012-2023\/APG%20Auditing%20Climate%20Change%20issues%20FINAL%203-19-2024.pdf\" target=\"_blank\" rel=\"noopener\">ISO and IAF guidance on the amendment<\/a> clarifies the need to determine whether climate change is a relevant issue for the QMS.<\/p>\n<p>When preparing for the transition, review this assessment in light of the current circumstances. Supply disruptions, storage conditions, resource availability or customer requirements are examples of situations that may warrant attention.<\/p>\n<p>This does not mean assuming that every organisation faces the same impacts. The analysis should be proportionate to the context, the products and services, and the relevant interested parties. When an organisation concludes that the issue is not relevant, it should be able to explain the assessment supporting that conclusion.<\/p>\n<h3>5. More guidance on interpreting the requirements<\/h3>\n<p>ISO 9001:2026 includes a revised Annex A, with explanations of concepts, terminology and the application of requirements. According to <a href=\"https:\/\/www.dqsglobal.com\/en\/explore\/focus-area\/iso-9001-revision-at-a-glance\" target=\"_blank\" rel=\"noopener\">DQS<\/a>, the annex is informative and does not add obligations.<\/p>\n<p>Consult it during the gap assessment, particularly where there are questions of interpretation. For organisations with integrated management systems, the transition is also an opportunity to review common processes such as internal audits, document management, objective setting and management review.<\/p>\n<p>Closer alignment with the harmonised structure of management system standards can facilitate this integrated analysis. However, the organisation should confirm how each requirement applies to its system and avoid assuming that similar processes automatically produce the same evidence.<\/p>\n<h2>Which areas of the organisation should be involved?<\/h2>\n<p>The transition should not be limited to the quality manager. Changes related to culture, ethics, strategy, risks and opportunities require input from different functions.<\/p>\n<ul>\n<li><strong>Top management:<\/strong> should participate in setting priorities, ensuring strategic alignment and assessing the resources required.<\/li>\n<li><strong>Process owners:<\/strong> should identify the impacts on the activities they manage and ensure that the changes are implemented.<\/li>\n<li><strong>Human resources:<\/strong> can support the analysis of competencies, awareness, training and internal communication.<\/li>\n<li><strong>Purchasing and supplier management:<\/strong> should assess whether there are impacts on supplier selection, monitoring or performance criteria.<\/li>\n<li><strong>Sales and customer support teams:<\/strong> can provide information on expectations, complaints and opportunities for improvement.<\/li>\n<li><strong>Internal auditors:<\/strong> should understand the changes so that they can assess not only the documentation, but also the implementation and effectiveness of practices.<\/li>\n<\/ul>\n<p>Involvement should be proportionate to the size and complexity of the organisation. The aim is not to create a parallel structure for the transition, but to integrate the new considerations into existing management mechanisms.<\/p>\n<h2>What is the transition deadline for ISO 9001:2026?<\/h2>\n<p>ISO indicates that certified organisations will need to complete the transition within the timeframe defined by their certification cycle and recommends contacting their certification body. As of the date of the sources used in this article, no general deadline had been confirmed in the IAF transition rules.<\/p>\n<p>Publication of the new edition does not automatically invalidate existing certificates. Their continued validity remains subject to the applicable certification conditions and any transition rules subsequently communicated by the relevant bodies.<\/p>\n<p>Confirm the following with your certification body:<\/p>\n<ul>\n<li>When it will be able to conduct the audit against the new edition.<\/li>\n<li>Whether the transition can coincide with an audit that is already scheduled.<\/li>\n<li>What information you will need to provide.<\/li>\n<li>Whether additional audit time will be required.<\/li>\n<li>Which formal dates and conditions apply to your certification cycle.<\/li>\n<\/ul>\n<p>Even without assuming an unconfirmed deadline, it is advisable to begin preparations in good time. The organisation needs time to interpret the requirements, implement the adjustments, assess their effectiveness and correct any nonconformities before the audit.<\/p>\n<h2>How to prepare for the ISO 9001:2026 transition in six steps<\/h2>\n<h3>1. Understand the new edition<\/h3>\n<p>Obtain the standard and identify the changes that apply to your QMS. Use technical summaries to support your reading, but always confirm the requirements in the normative text. Record any questions that need to be clarified with consultants, auditors or the certification body.<\/p>\n<h3>2. Conduct a gap assessment of the current system<\/h3>\n<p>Compare the requirements with existing practices. For each difference, record what needs to be adjusted, who will be responsible, the internal deadline and what evidence will allow the implementation to be assessed.<\/p>\n<p>The assessment should distinguish between an actual gap, an opportunity for improvement and a simple need for clarification. This distinction helps avoid unnecessary changes and allows resources to be focused on the areas with the greatest impact.<\/p>\n<h3>3. Set priorities and a schedule<\/h3>\n<p>Organise actions by importance and effort. Pay particular attention to matters that require the involvement of several teams or behavioural changes, as these need time to produce results.<\/p>\n<p>Include monitoring milestones before the transition audit. This will allow the organisation to verify progress and adjust the plan without leaving every decision until the end.<\/p>\n<h3>4. Involve management and teams<\/h3>\n<p>Explain the changes using examples suited to each function. Top management should participate in decisions and provide the necessary resources; teams should understand the impact on their work.<\/p>\n<p>Communication should explain why a particular change is necessary and how it will be implemented. Short sessions integrated into regular meetings may be more effective than generic communication that is unrelated to actual processes.<\/p>\n<h3>5. Verify the effectiveness of the changes<\/h3>\n<p>Include the amended requirements in the internal audit programme and monitor progress during management review. Look for evidence of implementation and results, as well as updated documentation.<\/p>\n<p>Interviews, observation of activities, analysis of indicators and sampling of records can help verify whether the new practices have been understood and embedded. When results do not meet expectations, review the action instead of simply producing more documentation.<\/p>\n<h3>6. Prepare for the transition audit<\/h3>\n<p>Coordinate the schedule with the certification body. Before the audit, confirm that the actions have been implemented, responsibilities are clear and there is sufficient time to resolve outstanding matters.<\/p>\n<p>Organise evidence in a simple way that is consistent with the processes. There is no need to create a separate file when the information is already available in the systems used by the organisation.<\/p>\n<h2>Mistakes to avoid<\/h2>\n<ul>\n<li><strong>Limiting the work to documentation.<\/strong> Procedures should reflect practices that have actually been implemented.<\/li>\n<li><strong>Creating unnecessary bureaucracy.<\/strong> Adapt existing tools whenever they meet the requirements.<\/li>\n<li><strong>Making the quality manager solely responsible for the transition.<\/strong> Leadership and process owners need to participate.<\/li>\n<li><strong>Leaving verification until the end.<\/strong> Assessing adjustments in advance makes it possible to correct problems before the audit.<\/li>\n<li><strong>Treating every issue as having the same priority.<\/strong> The plan should reflect the risks, opportunities and specific context of the organisation.<\/li>\n<li><strong>Basing the schedule on unconfirmed deadlines.<\/strong> Validate the transition conditions with your certification body.<\/li>\n<\/ul>\n<h2>Frequently asked questions<\/h2>\n<h3>Is it necessary to rebuild the entire quality management system?<\/h3>\n<p>The work should begin with a gap assessment. Retain the processes that work and adjust the areas where there are differences in relation to the new edition. A revision of the standard does not, in itself, mean that all documentation must be replaced or every process changed.<\/p>\n<h3>Does ISO 9001:2026 require the use of artificial intelligence?<\/h3>\n<p>No. According to <a href=\"https:\/\/www.dqsglobal.com\/en\/explore\/focus-area\/iso-9001-revision-at-a-glance\" target=\"_blank\" rel=\"noopener\">DQS<\/a>, the standard retains a technology-neutral approach, without a specific requirement for artificial intelligence. If the organisation uses AI in activities relevant to quality, it should assess the effects of that use on its QMS.<\/p>\n<h3>Is it mandatory to keep separate risk and opportunity registers?<\/h3>\n<p>The distinction between the two topics does not, in itself, determine the format of the records. The chosen tool should make it possible to understand decisions, monitor actions and assess results.<\/p>\n<h3>Is it necessary to train everyone?<\/h3>\n<p>The organisation should assess who is affected by the changes and what knowledge or competencies are required. The response may involve training, awareness, communication or on-the-job support, depending on the functions involved and the impact of the changes.<\/p>\n<h2>Resources you may find useful<\/h2>\n<ul>\n<li><a href=\"https:\/\/icompliance.eu\/en\/nis2-implementation-in-portugal-practical-roadmap-for-compliance-2026\/\" target=\"_blank\" rel=\"noopener\">NIS2 implementation in Portugal (2026)<\/a><\/li>\n<li><a href=\"https:\/\/icompliance.eu\/en\/compliance\/\" target=\"_blank\" rel=\"noopener\">Compliance<\/a><\/li>\n<li><a href=\"https:\/\/icompliance.eu\/en\/implementation-of-iso-27001\/\" target=\"_blank\" rel=\"noopener\">ISO 27001 implementation<\/a><\/li>\n<\/ul>\n<p><strong><a href=\"https:\/\/icompliance.eu\/en\/resources\/\" target=\"_blank\" rel=\"noopener\">View all resources<\/a><\/strong><\/p>\n<h2 id=\"recursos-relacionados\">Resources you may find useful<\/h2>\n<ul>\n<li><a href=\"https:\/\/icompliance.eu\/en\/nis2-implementation-in-portugal-practical-roadmap-for-compliance-2026\/\">NIS2 implementation in Portugal (2026)<\/a><\/li>\n<li><a href=\"https:\/\/icompliance.eu\/en\/compliance\/\">Compliance<\/a><\/li>\n<li><a href=\"https:\/\/icompliance.eu\/en\/compliance-management\/\">Compliance Management 2026: Proven Guide<\/a><\/li>\n<\/ul>\n<p><strong><a href=\"https:\/\/icompliance.eu\/en\/resources\/\">See all resources<\/a><\/strong><\/p>\n<h2>How iCompliance can help<\/h2>\n<p><a href=\"https:\/\/icompliance.eu\/en\/\" target=\"_blank\" rel=\"noopener\">iCompliance<\/a> supports your organisation in assessing gaps against ISO 9001:2026, defining the transition plan, reviewing documentation and preparing teams.<\/p>\n<p>Our support builds on the existing system and the organisation\u2019s needs, focusing on the practical application of the requirements, verification of the effectiveness of changes and preparation for the audit.<\/p>\n<p>Contact iCompliance to assess your QMS and plan the transition to ISO 9001:2026.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Learn what changes in ISO 9001:2026, from quality culture to risks and opportunities, and how to prepare your QMS transition.<\/p>\n","protected":false},"author":1,"featured_media":8082,"comment_status":"open","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"_ice_seo_score":77,"_ice_review":"published","footnotes":""},"categories":[37],"tags":[],"class_list":["post-8081","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-compliance-iso"],"_links":{"self":[{"href":"https:\/\/icompliance.eu\/en\/wp-json\/wp\/v2\/posts\/8081","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/icompliance.eu\/en\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/icompliance.eu\/en\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/icompliance.eu\/en\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/icompliance.eu\/en\/wp-json\/wp\/v2\/comments?post=8081"}],"version-history":[{"count":2,"href":"https:\/\/icompliance.eu\/en\/wp-json\/wp\/v2\/posts\/8081\/revisions"}],"predecessor-version":[{"id":8086,"href":"https:\/\/icompliance.eu\/en\/wp-json\/wp\/v2\/posts\/8081\/revisions\/8086"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/icompliance.eu\/en\/wp-json\/wp\/v2\/media\/8082"}],"wp:attachment":[{"href":"https:\/\/icompliance.eu\/en\/wp-json\/wp\/v2\/media?parent=8081"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/icompliance.eu\/en\/wp-json\/wp\/v2\/categories?post=8081"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/icompliance.eu\/en\/wp-json\/wp\/v2\/tags?post=8081"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}