Services
Initial Certification
Independent Stage 1 and Stage 2 audits leading to a certification decision and an ISO certificate valid for three years, subject to surveillance.
- Audit programme covering the full three year certification cycle
- Stage 1 audit with a written readiness report
- Stage 2 audit by auditors competent in your sector
- Clear audit report with graded findings and objective evidence

Overview
Independent Stage 1 and Stage 2 certification audits
Initial certification is the route by which an organisation that has implemented a management system obtains its first certificate from Hexa Certifications. The process follows ISO/IEC 17021-1 and is carried out in two stages, so that readiness is confirmed before the full assessment of how the system works in practice. Our role is to assess objectively against the chosen standard, never to design or write the system for you.
Stage 1 reviews your documented information, scope, site conditions, legal and regulatory context and readiness for Stage 2. Stage 2 then evaluates whether the management system has been implemented effectively across the agreed scope, through interviews, observation and sampling of records. Any nonconformities are reported clearly so that you can determine and carry out your own corrections and corrective actions.
Once the audit evidence is complete, a certification decision is made by competent personnel who were not involved in the audit. If the decision is positive, we issue a certificate that is valid for three years, provided surveillance audits are completed each year and the system continues to meet the requirements of the standard. Customers and other interested parties can ask us to confirm the status and scope of your certificate at any time.

How it works
Initial Certification, step by step
Every stage is planned and confirmed with you in advance, so your team knows exactly who is coming, when, and what they need to see.
- 1
Application and proposal
You tell us about your organisation, scope, sites and headcount. We determine audit time in line with the relevant IAF mandatory documents and confirm the audit programme in writing.
- 2
Stage 1 audit
We review your documented information, scope, processes and readiness, and identify any areas of concern that could be classified as nonconformities at Stage 2.
- 3
Stage 2 audit
Auditors evaluate the implementation and effectiveness of the management system on site or remotely where appropriate, sampling activities, records and interviews across the scope.
- 4
Corrective action
Where nonconformities are raised, you analyse causes and submit corrections and corrective actions. Major nonconformities must be addressed and verified before a certificate can be granted.
- 5
Certification decision
An independent reviewer who did not take part in the audit examines the audit report and evidence and makes the decision to grant, or not grant, certification.
- 6
Certificate issued
Your certificate states the standard, scope and sites covered and is valid for three years, subject to successful annual surveillance audits.
- Organisations seeking their first ISO certificate
- Businesses asked by customers or tenders for certified management systems
- Companies extending certification to a new standard
- Organisations whose previous certificate has lapsed beyond restoration
- Multisite businesses seeking certification across several locations
Available for
Initial Certification for every standard
This service is available for every standard we certify. Choose one to learn more.
Quality
ISO 9001:2026Quality Management
ISO 9001:2026 sets out the requirements for a quality management system. Published in September 2026, it replaces ISO 9001:2015 and keeps the same core approach. It asks an organisation to understand its context and interested parties, plan its processes around risks and opportunities, and show that it consistently provides products and services that meet customer and applicable statutory and regulatory requirements. It is the most widely used management system standard and applies to organisations of any size or sector, from sole manufacturers to national service providers.
- Meet tender and supplier requirements
- Consistent processes
- Fewer errors and complaints
- Risk based planning

Environment & Energy
ISO 14001:2026Environmental Management
ISO 14001:2026, published in April 2026 to replace the 2015 edition, specifies the requirements for an environmental management system. It helps an organisation identify the environmental aspects of its activities, products and services, understand its compliance obligations, and manage significant impacts through planning, operational control and evaluation. The standard takes a life cycle perspective, so organisations consider stages they can control or influence, such as purchasing, transport, use and end of life treatment, as well as their own sites.
- Supply chain and tender credibility
- Structured legal compliance
- Control of significant impacts
- Resource and waste efficiency

Health & Safety
ISO 45001:2018Occupational Health and Safety Management
ISO 45001:2018 sets out requirements for an occupational health and safety management system. Its aim is to prevent work related injury and ill health and to provide safe and healthy workplaces. The standard places strong emphasis on leadership, the consultation and participation of workers, hazard identification and the hierarchy of controls. It replaced OHSAS 18001 and follows the Harmonized Structure, so it integrates readily with ISO 9001 and ISO 14001.
- Prequalification and tenders
- Worker involvement
- Systematic hazard control
- Clear legal oversight

Information & Technology
ISO/IEC 27001:2022Information Security Management
ISO/IEC 27001:2022 specifies requirements for an information security management system (ISMS). It requires an organisation to assess information security risks to the confidentiality, integrity and availability of information, select controls to treat them and manage those controls through a continual cycle of monitoring and review. Annex A lists 93 reference controls in four themes: organisational, people, physical and technological. Each organisation compares its chosen controls against Annex A and records the outcome in a Statement of Applicability.
- Answer security questionnaires
- Risk based security
- Supports data protection duties
- Management oversight

Environment & Energy
ISO 50001:2018Energy Management
ISO 50001:2018 specifies requirements for an energy management system (EnMS). It requires an organisation to understand how it uses and consumes energy, identify significant energy uses, set an energy baseline and energy performance indicators, and plan actions to improve energy performance. Unlike some other management system standards, ISO 50001 requires an organisation to demonstrate continual improvement in energy performance itself, not only in the management system.
- ESOS compliance route
- Measured energy performance
- Focus on significant uses
- Cost control

Resilience & Governance
ISO 22301:2019Business Continuity Management
ISO 22301:2019 specifies requirements for a business continuity management system (BCMS). It helps an organisation prepare for, respond to and recover from disruptive incidents when they occur. The core of the standard sits in clause 8, which requires a business impact analysis and risk assessment, business continuity strategies and solutions, documented plans and procedures, an exercise programme and evaluation of business continuity capability. It follows the Harmonized Structure and integrates with other management system standards.
- Evidence for customers
- Clear recovery priorities
- Tested plans
- Understanding dependencies

Sector specific
ISO 22000:2018Food Safety Management
ISO 22000:2018 specifies requirements for a food safety management system for any organisation in the food chain, from feed and primary production through processing, storage, transport, retail and food service, as well as packaging and equipment suppliers. It combines the Harmonized Structure management system clauses with HACCP principles from Codex Alimentarius, prerequisite programmes (PRPs) and interactive communication across the food chain. The standard uses two linked Plan, Do, Check, Act cycles: one for the management system and one for operational hazard control.
- Structured hazard control
- Applies across the food chain
- Management system discipline
- Communication across the chain

Sector specific
ISO 13485:2016Medical Devices Quality Management
ISO 13485:2016 specifies requirements for a quality management system where an organisation needs to demonstrate its ability to provide medical devices and related services that consistently meet customer and applicable regulatory requirements. It applies to manufacturers and to organisations involved in other stages of the device life cycle, such as design, distribution, installation, servicing, sterilisation and component supply. The standard places particular emphasis on risk management, process validation, traceability and regulatory reporting.
- Supports regulatory submissions
- Supply chain requirements
- Risk management throughout
- Validated processes

Information & Technology
ISO/IEC 20000-1:2018IT Service Management
ISO/IEC 20000-1:2018 specifies requirements for establishing, implementing, maintaining and continually improving a service management system (SMS). It covers the planning, design, transition, delivery and improvement of services to meet agreed requirements. Clause 8 sets out the operational processes, grouped into service portfolio, relationship and agreement, supply and demand, service design, build and transition, resolution and fulfilment, and service assurance. The 2018 edition follows the Harmonized Structure, which allows integration with ISO/IEC 27001 and ISO 9001.
- Procurement credibility
- Consistent service delivery
- Clear service agreements
- Controlled change

Information & Technology
ISO/IEC 42001:2023Artificial Intelligence Management
ISO/IEC 42001:2023 is the first international management system standard for artificial intelligence. It specifies requirements for establishing, implementing, maintaining and continually improving an AI management system (AIMS) within an organisation that develops, provides or uses AI systems. It requires AI risk assessment, AI risk treatment and AI system impact assessment, considering effects on individuals, groups and society. Annex A provides reference controls covering areas such as AI policy, resources, impact assessment, the AI system life cycle, data and third party relationships.
- Evidence of responsible AI governance
- Structured risk and impact assessment
- Clear roles and accountability
- Life cycle controls

Resilience & Governance
ISO 37001:2025Anti Bribery Management
ISO 37001 specifies requirements for an anti bribery management system. It helps an organisation prevent, detect and respond to bribery, whether by the organisation, its personnel or business associates acting on its behalf, and bribery of the organisation. Requirements include an anti bribery policy, top management and governing body oversight, an anti bribery compliance function, bribery risk assessment, due diligence, financial and nonfinancial controls, gifts and hospitality controls, and processes for raising and investigating concerns. The second edition, ISO 37001:2025, was published in February 2025.
- Supports adequate procedures
- Risk based controls
- Due diligence on third parties
- Clear governance oversight

FAQs
Initial Certification: your questions
What is the difference between Stage 1 and Stage 2?
Stage 1 confirms that your management system is ready to be assessed. It focuses on documented information, scope, site conditions, legal requirements and planning for Stage 2. Stage 2 is the main evaluation, where auditors test whether the system has been implemented and is effective in practice by interviewing staff, observing work and sampling records across the certified scope.
How long is the gap between Stage 1 and Stage 2?
There is no single fixed gap. It depends on how ready the system is and on any concerns raised at Stage 1 that need attention before Stage 2. Some organisations proceed within a few weeks, while others need longer to resolve issues. The gap should not be so long that the Stage 1 findings are no longer valid, and we will agree timing with you.
Do we need to have run the system for a period before the audit?
Auditors need sufficient evidence that the system is operating, which normally means records showing that processes have been followed, at least one internal audit has been completed across the scope and a management review has taken place. Without this evidence it is difficult to demonstrate effective implementation at Stage 2.
What happens if a major nonconformity is raised?
A major nonconformity prevents certification until it has been addressed. You will need to determine the cause, take correction and corrective action, and provide evidence that we can verify, sometimes through a short follow up visit. If verification cannot be completed within the timeframe set out in ISO/IEC 17021-1, typically six months from the last day of Stage 2, a further Stage 2 audit is required.
Who makes the certification decision?
The decision is made by competent personnel at Hexa Certifications who were not involved in your audit. They review the audit report, the evidence gathered and any corrective action submissions. Separating the audit from the decision is a core requirement of ISO/IEC 17021-1 and helps protect the impartiality and consistency of certification.
How long is the certificate valid?
Certificates are issued for a three year cycle. Validity depends on successful surveillance audits during that period, normally at least once each calendar year. Before the three years end, a recertification audit is needed to renew the certificate for a further cycle. Certificates can be suspended or withdrawn if surveillance is not carried out or serious issues are found.
Will you help us write our policies and procedures?
No. Certification bodies must not provide management system consultancy to the organisations they certify, as this would compromise impartiality. We can explain the certification process and what auditors will look for, but designing, writing or implementing your system must be done by your own team or an independent adviser with no link to our audit work.
Can audits be carried out remotely?
Some audit activities can be conducted remotely where this is appropriate and permitted by the relevant IAF guidance, for example document review or interviews with staff at other locations. Activities that need direct observation, such as operational sites, production or construction work, are normally audited on site. We confirm the method for each activity in your audit plan.
Certificate verification
Check a Hexa certificate
Need to know whether a supplier's certificate is current? Customers, buyers and other interested parties can ask us to confirm the details held in our records.
We confirm the organisation name, certificate number, ISO standard, certified scope, status, and issue and expiry dates.
More services
Explore our other services
- Surveillance AuditsAnnual audits that keep your certificate validLearn more
- Recertification AuditsRenew your certificate for a further three year cycleLearn more
- Certificate TransferMove an existing accredited certificate to HexaLearn more
- Integrated Management SystemsCombined audits for several ISO standardsLearn more
- Readiness AssessmentAn optional readiness check before certificationLearn more
- Management System TrainingPublic awareness and internal auditor coursesLearn more
- Certificate VerificationConfirm a Hexa certificate is genuine and currentLearn more
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Get a fixed, three year certification quote
Tell us about your organisation and the standards you need. We will confirm audit days, scope and dates in writing, with no obligation.


