Europe-wide ISO and compliance support
Describe your standard, sector, location and deadline. We help route your request to suitable consultants, internal auditors, laboratories, certification bodies or CE-marking specialists—without confusing advisory work with independent conformity assessment.
- Standard-specific project routing
- Remote and on-site options
- Consulting and independent audit paths kept separate
Project matching
Tell us what you need
Choose the standard or regulatory area first. The next step will show only services that fit that route.
No certification claim is created by submitting this form.
- 1Standard
- 2Service
- 3Project details
Step 1 of 3
Which standard or compliance area applies?
Search by number, topic or industry.
Management system standards
Implementation, internal audit, certification readiness and independent certification-body routes.
Industry schemes and accreditation
Routes with scheme-specific recognition, laboratory competence or sector-specific certification rules.
EU product and market-access compliance
Product legislation, technical documentation, testing and third-party conformity assessment where required.
Climate, risk and advisory frameworks
Verification, reporting and non-certifiable guidance routes that need different provider types.
Choose “Other / not sure” below, and describe the product, industry or customer requirement in the final step.
Step 2 of 3
What type of support do you need?
Step 3 of 3
Describe your project and request matches
Read how your information is handled in the Privacy Policy. Submitting a request does not create an engagement or guarantee that a suitable provider is available.
Choose the correct provider
Consultant, auditor, certification body or notified body?
These roles solve different problems. Separating them improves quote quality, protects independence and reduces the risk of paying for a service that cannot deliver the outcome you need.
ISO consultant
Helps design, document, implement and improve your management system. A consultant can prepare you for certification but should not issue your independent certificate.
Internal auditor or gap assessor
Tests readiness, identifies nonconformities and supports corrective action. This is not the same as the independent certification audit.
Certification or accreditation body
Performs independent conformity assessment. Check the body’s competence, recognition, accreditation status and scope for your standard and sector.
Notified body or testing laboratory
A notified body participates only when the applicable EU legislation requires third-party assessment. A competent laboratory may perform product, material or calibration testing.
Current standards intelligence
Key 2026 changes worth scoping now
ISO 14001:2026 is the current edition
Organizations certified to the previous edition should plan transition activity with their certification body and implementation support team.
ISO 9001 revision support
The sixth edition is in final publication work. New implementation projects should avoid building a system that cannot absorb the coming transition efficiently.
ISO 37001:2025 replaced the 2016 edition
Anti-bribery management projects should be scoped against the current edition and the organization’s applicable legal and contractual obligations.
Standards and regulatory coverage
Popular ISO consulting and compliance projects in Europe
The correct route depends on whether you need a certifiable management system, laboratory accreditation, product conformity, greenhouse-gas assurance or a non-certifiable guidance framework.
Quality and sector QMS
ISO 9001, ISO 13485, IATF 16949 and IAQG 9100 projects may include implementation, process mapping, internal audits, supplier controls, audit readiness and certification-body selection.
Information security and AI governance
ISO/IEC 27001 and ISO/IEC 42001 work can cover risk assessment, statements of applicability, controls, governance, internal audit and readiness for independent certification.
Environment, energy and safety
ISO 14001, ISO 50001 and ISO 45001 support integrated management systems covering environmental performance, energy performance and occupational health and safety.
EU product compliance and CE marking
Projects may require legislation scoping, harmonised standards, risk assessment, technical documentation, testing, declarations and notified-body involvement where the conformity route requires it.
Laboratory competence and GHG assurance
ISO/IEC 17025 is normally used for laboratory accreditation, while ISO 14064 projects may involve emissions inventories, data controls and independent validation or verification.
Risk and social responsibility guidance
ISO 31000 and ISO 26000 can support governance, maturity assessment and implementation, but they are guidance standards and should not be sold as accredited certification.
A clearer buying process
How expert matching works
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1
Define the outcome
Tell us the standard, service type, sites, headcount, current maturity, language, market and deadline.
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2
Route to the right provider type
We distinguish implementation support from independent certification, accreditation, testing, validation or notified-body work.
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3
Compare relevant responses
Where suitable providers are available, review scope, competence, exclusions, deliverables, timing, travel assumptions and commercial terms.
Quote quality checklist
What a professional ISO or compliance quote should state
- The standard, edition, scheme or legislation covered.
- Sites, legal entities, products, processes and exclusions.
- Consulting days, audit days, testing scope or assessment modules.
- Remote versus on-site delivery and travel assumptions.
- Named deliverables, milestones and client responsibilities.
- Provider competence, recognition and applicable accreditation scope.
- Independence boundaries between consulting and certification.
- Fees, taxes, retesting, surveillance and recurring costs.
Frequently asked questions
ISO consultant and auditor FAQs
Does ISO certify companies or issue ISO certificates?
No. ISO develops standards. Independent certification bodies perform certification and issue certificates. Organizations are certified to a standard; they are not “certified by ISO.”
Is an “accredited ISO auditor” the right term?
Usually not as a blanket description. Accreditation generally applies to certification, inspection, testing, calibration or verification bodies and their defined scopes. Individual auditors may hold qualifications and sector competence, but you should verify the organization, scheme and scope behind the audit.
Can the same consultant implement the system and issue the certificate?
Independent certification must be separated from consulting. A consultant may prepare your organization, but the certification decision belongs to an independent certification body operating under its applicable impartiality rules.
Are ISO 31000 and ISO 26000 certifiable?
No. They are guidance standards. They can support implementation, benchmarking, governance and audit programmes, but they should not be marketed as accredited certification standards.
Do all products need a notified body for CE marking?
No. The applicable EU legislation determines the conformity-assessment route. Some products permit manufacturer self-assessment; higher-risk or specifically regulated products may require a notified body. CE marking is not a universal certificate issued by one central EU authority.
How much does ISO consulting or certification cost?
Price depends on the standard, number of employees and sites, operational complexity, risk, current readiness, required languages, travel, certification scope and whether testing, accreditation or notified-body work is involved. A useful quote should state assumptions and recurring costs clearly.
How long does ISO certification take?
There is no reliable universal duration. Timing depends on readiness, leadership availability, process maturity, evidence and records, corrective actions, audit scheduling and scope. A credible provider should give a phased plan after reviewing your actual starting point.
Can projects be delivered remotely across Europe?
Many implementation, documentation, training and internal-audit activities can be delivered remotely. On-site work may still be appropriate or required for operational audits, product testing, physical inspections, laboratory assessments or scheme-specific rules.
Independent information sources
For formal definitions and current regulatory routes, consult ISO’s certification guidance and the European Union’s CE-marking guidance. Always verify the current edition, applicable legislation and provider scope before contracting.