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.