Validation

Our Offering:

Validation of temperature, humidity and environment

To ensure that production and storage environments maintain the correct conditions, regular validation is required. We help you verify that, for example, climate chambers, cold rooms, freezers or incubators meet the defined requirements for temperature, humidity and airflow. Common applications include:

• Climate chambers and environmental test equipment
• Storage spaces (refrigerated/freezer/warehouse)
• Medical devices
• Incubators and sensitive environments

We perform measurements against tolerance intervals and provide validation reports that can be used during audits and follow-ups.

Validation of sterilization processes

In healthcare and pharmaceutical environments, correct sterilization is critical. We validate that autoclaves and dry sterilizers meet the requirements by measuring and verifying:

• Temperature
• Pressure
• Time
• Humidity

Validation ensures the equipment is safe for use and that processes comply with GMP and other regulatory requirements.

Validation of production equipment and process systems

To maintain quality and process safety in manufacturing, validation of production equipment is essential. We offer qualification and performance verification of equipment such as:

• Packaging lines
• Tablet machines
• Piping systems and pressurized facilities

We inspect temperature, pressure, flow, dosing and other parameters in accordance with current standards – from FAT and SAT to IQ, OQ and PQ.

Validation of cleanrooms and particle measurement

We validate cleanrooms according to ISO 14644-1 and -2 by measuring particle counts, airflow and pressure differentials. This is critical in industries where contamination risk must be minimized, such as:

• Pharmaceutical and medical technology
• Biotechnology and microelectronics
• Food production
• Sensitive assembly

We ensure that the environment meets classification and cleanliness level requirements.