FAQ

A QMS is a structured system of procedures, processes, and responsibilities for achieving quality policies and objectives. It helps organizations consistently meet customer and regulatory requirements and improve their overall performance.

QMS certification, such as ISO 9001, demonstrates your commitment to quality, enhances customer trust, improves internal processes, and opens doors to new business opportunities—especially with clients who require certified suppliers.

We offer certification services for various QMS standards, including but not limited to:ISO 9001: Quality ManagementISO 13485: Quality Management for Medical DevicesISO 22000: Food Safety Management Our expert auditors ensure your system aligns with international standards.

The certification process typically includes:Application & ContractStage 1 Audit – Document review & readiness assessmentStage 2 Audit – On-site audit to verify complianceCertification DecisionOngoing Surveillance Audits (usually annually)

The duration depends on the size and complexity of your organization. On average, the process may take 2 to 6 months, including preparation, documentation, internal audits, and our certification audit.

No, QMS certifications are generally valid for three years, subject to successful annual surveillance audits. A recertification audit is required at the end of the cycle to maintain certification.