Commissioning & validation

Lab commissioning and validation

Precision assurance

To uphold a high standard, laboratory commissioning and validation emerge as indispensable pillars of assurance. These processes, grounded in exactitude and adherence to stringent protocols, serve as the linchpin for laboratory operations, ensuring unparalleled reliability, regulatory compliance, and data integrity.

Our methodology begins with a comprehensive assessment of your laboratory’s unique requirements, coupled with a deep understanding of regulatory standards and guidelines. Leveraging this insight, we craft a tailored validation and commissioning plan that aligns with your objectives and prioritizes precision at every step.

Why choose our commissioning and validation services?

By paying careful attention to these technical requirements and specifications in the first phase, you can create a laboratory environment that promotes innovation, collaboration, and safety for researchers and scientists alike.

Diverse industry expertise

Extensive experience in commissioning and validation spanning across multiple industries and laboratory types ensures adept handling of diverse project requirements.

QA commitment

Dedicated to upholding the highest standards of quality, compliance, and customer satisfaction, ensuring every project meets regulatory requirements and exceeds expectations.

Certified excellence

Backed by relevant certifications, accreditations, and industry affiliations, providing assurance of our proficiency, credibility, and adherence to industry best practices.

Quality assurance

Our quality assurance services

Our experienced team specializes in the validation and commissioning of laboratory equipment and facilities. From initial setup to final testing, we ensure that your laboratory meets all regulatory requirements and industry standards.

This involves the qualification of laboratory equipment to ensure that it operates within specified parameters and produces accurate results. Equipment qualification typically includes installation qualification (IQ), operational qualification (OQ), and performance qualification (PQ) to verify that the equipment is properly installed, functions as intended, and consistently produces reliable results.

With our thorough quality assurance protocols, we help you maintain compliance with regulatory agencies and uphold the highest standards of quality and safety in your laboratory operations.

Process validation is essential for laboratories involved in manufacturing or production processes, such as pharmaceutical manufacturing or food processing laboratories. It involves validating manufacturing processes to ensure consistency, reliability, and compliance with quality standards, regulatory requirements, and product specifications.

In laboratories where computerized systems are used for data acquisition, processing, and analysis, CSV is essential to ensure the integrity, security, and reliability of electronic records and data. This involves validating software applications, databases, and hardware components to ensure compliance with regulatory requirements and data integrity standards.

Facility validation ensures that laboratory facilities meet regulatory requirements and are suitable for their intended use. This includes validation of facility design, construction, utilities, HVAC systems, and environmental controls to ensure compliance with Good Manufacturing Practice (GMP) and other regulatory standards.

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Get in touch

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Our Office

Kieleberg 1

3740 Munsterbilzen


Call us

+32 (0)473 69 25 41

E-mail us

Working Hours

Mon – Fri

08:30 AM – 17:00 PM