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Accredited ISO 9001 certification that demonstrates to clients, tender committees and regulators that your organisation consistently meets customer and regulatory requirements.

Accredited by EGAC, the Egyptian Accreditation Council
Management System Certification · ISO/IEC 17021-1
ISO 9001, ISO 14001, ISO 45001, ISO/IEC 27001, ISO 22000, ISO 50001 and ISO 21001, audited in accordance with ISO/IEC 17021-1 and the applicable sector rules: ISO/IEC 17021-2, ISO/IEC 17021-3, ISO/IEC 17021-10, ISO 22003-1, ISO 50003 and ISO/IEC 27006-1.
Accreditation details

Schedule number to be added
ISO 9001 is the internationally recognised standard for quality management systems. It specifies the requirements for an organisation to plan, operate, monitor and improve its processes so that products and services consistently meet customer requirements and applicable statutory and regulatory requirements.
The standard does not prescribe how a business should operate. It requires the organisation to understand its context and interested parties, define its processes, address risks and opportunities, measure performance and pursue continual improvement. Certification is the independent confirmation, by an accredited body, that the system conforms to these requirements and is effectively implemented.
Accredited certification is independent evidence that your management system conforms to the standard and is effective in practice.

The outcomes organisations most commonly seek from certification.
The standard applies to organisations of any size and sector. Certification is particularly valuable if you:
Answer six questions to assess your readiness for the certification audit.
Questions left:
Ready for the certification audit
Your system covers the elements auditors examine first. The next step is to request a quotation and schedule the Stage 1 audit.
Request a QuotationApproaching readiness
You have a sound basis. Complete the open points and build records of operation, then request a quotation and a proposed timeline.
Request a Quotation and TimelineEarly stage
Your system is at an early stage. An advisor can explain the certification process and a realistic timeline.
Speak to an AdvisorThe requirements are set out in clauses 4 to 10, following the Plan, Do, Check, Act cycle. Auditors will expect to see the following documented information.
Key documented information
Each stage is planned and confirmed with you in advance.
You provide details of your scope, personnel and sites. We determine the audit time and issue a fixed quotation and certification agreement.
You: complete a short application. We: respond within one business day.
The audit team reviews your documented information, site conditions and readiness, and confirms the plan for Stage 2.
You: provide your documentation. We: report any areas of concern.
The audit team evaluates on site how effectively the management system is implemented.
You: host the audit. We: present findings at the closing meeting.
A competent reviewer, independent of the audit team, reviews the audit and makes the certification decision.
You: address any nonconformities. We: issue your certificate.
The fee is determined mainly by audit time, which is calculated in accordance with IAF MD 5 from the number of personnel, the number of sites and the complexity of your activities. This approach keeps fees consistent and comparable.
The full cost of the cycle, confirmed before you commit
Stage 1 and Stage 2 audits. Issue of the certificate. Two annual surveillance audits. No undisclosed charges.
Request a Fixed QuotationISO 9001 follows the harmonised structure of ISO management system standards, so it can be audited together with other standards.
Transfer your ISO 9001 certificate to GQCL
A valid accredited certificate held with another certification body can be transferred to GQCL after a pre-transfer review, in accordance with IAF MD 2, without restarting your certification cycle.
How Transfers Work
Yes. ISO 9001 applies to any organisation that provides products or services, regardless of size or sector, including consultancies, contractors, logistics providers, healthcare providers, technology companies and educational institutions.
A requirement may be determined as not applicable only where it cannot be applied within the scope of your management system, for example design and development where you do not design products or services. The justification must be documented, and it must not affect your ability to ensure the conformity of your products and services.
There is no fixed period, but the system must be fully implemented and producing records. Auditors expect to see a complete internal audit and a management review before the Stage 2 audit, normally supported by around three months of operating records.
Certification cannot be granted until a major nonconformity has been corrected and the correction verified, which may require a follow-up visit. Minor nonconformities require an accepted corrective action plan before the certification decision.
ISO 9001 has been revised, and the new edition is ISO 9001:2026. Certificates to ISO 9001:2015 remain valid throughout the transition period set by the accreditation bodies, normally three years. Certified clients receive a transition plan, and the transition audit is normally combined with a scheduled surveillance or recertification audit.
Once your management system is implemented and has operated long enough to produce records, including a complete internal audit and a management review, the certification process normally takes six to ten weeks from application to certificate. Your quotation sets out the proposed timeline.
Three years from the certification decision, subject to satisfactory annual surveillance audits. A recertification audit before expiry renews the certificate for a further three years.
No. As an accredited certification body, GQCL does not provide consultancy on the management systems it certifies, as ISO/IEC 17021-1 requires. We explain the requirements and the certification process clearly, and the Stage 1 audit identifies any areas of concern before Stage 2.
Yes. Audits, meetings and audit communication can be conducted in Arabic or English, according to your preference.