In the specialized field of industrial and cryogenic gas laboratories, strict compliance with the highest quality and accuracy standards is essential.
ISO 17025 is the world’s most recognized international standard for testing and calibration laboratories, ensuring technical competence and the reliability of laboratory results.

Sial Tamin Roham, with a team of qualified experts and proven experience in quality system implementation, supports you through every step of achieving ISO 17025 certification and establishing fully compliant laboratories.

The Importance of ISO 17025

ISO 17025 is the globally accepted benchmark for demonstrating the technical competence of testing and calibration laboratories.
Certification proves your laboratory’s ability to produce accurate, repeatable, and reliable results—a critical factor in earning the trust of clients and regulatory authorities.

Our Consulting Process

1. Initial Gap Assessment

• Comprehensive evaluation of the current laboratory setup.
• Identification of non-conformities against ISO 17025 requirements.
• Development of a roadmap for full compliance.
• Assessment covers equipment, personnel, procedures, and environmental conditions.

2. Quality Management System (QMS) Development

• Creation of a complete quality management framework.
• Documentation of all processes—from testing procedures to document control.
• Ensuring all requirements of the ISO 17025 standard are fully addressed.

3. Training & Capacity Building

• Staff training on ISO 17025 requirements, quality control methods, and testing techniques.
• Internal auditor training and designation of quality managers.
• Development of competency-based training plans.

4. Equipment Control & Calibration

• Establishing calibration schedules for all lab instruments.
• Implementing equipment tracking systems.
• Ensuring all measurements remain valid and traceable to recognized standards.

5. Method Validation

• Verification of testing methods for accuracy, precision, repeatability, and detection limits.
• Validation of non-standard methods with supporting evidence of performance.

6. Sample Management & Environmental Controls

• Implementation of storage and handling protocols for test samples.
• Monitoring of environmental parameters (temperature, humidity, etc.) to ensure result integrity.
• Continuous environmental tracking systems.

7. Internal Audits & Continuous Improvement

• Conducting regular internal audits to verify system effectiveness.
• Applying corrective and preventive actions to resolve non-conformities.
• Establishing a culture of continuous improvement.

8. Final Audit Preparation

• Pre-certification audit simulations to identify and resolve deficiencies.
• Support in document preparation and submission to certification bodies.

9. Post-Certification Support

• Ongoing system updates to match changes in the standard.
• Refresher training for staff and readiness for surveillance audits.