Validation

What is Validation? Why should we validate?

Validation is establishing documented evidence which provides a high degree of assurance that a specific process will Consistently produce a product meeting its pre-determined specifications and quality characteristics. Validation allows us to focus on our everyday business operations of making and selling quality products that also comply with regulatory requirements.

Ensure quality

Validation verifies that a system or process performs as expected, producing accurate and reliable results.

Confidence and trust

Validation builds stakeholder confidence in product reliability, fostering trust and ensuring effectiveness and compliance.

What We Validate?

We validate critical systems and equipment in pharmaceutical and biopharmaceutical settings, including:

Under Validation we conduct tests as follows:

Our Validation and Calibration Instruments are timely tested and calibrated according to the latest standards

Air Velocity Test

Ensuring accurate air velocity measurements for optimal system performance.

Non-Viable Particle Count Test

Testing for non-viable particle counts ensures environmental cleanliness compliance.

Smoke Pattern Test

Smoke pattern test evaluates airflow direction and integrity within controlled environments.

Light-Lux Intensity Test

Light-lux intensity test measures luminous flux to ensure proper lighting levels for safety and comfort.

Thermal Mapping

Temperature studies

PAO Filter Integrity Test

Ensuring accurate air velocity measurements for optimal system performance.

Recovery Test

Recovery test evaluates system or process resilience and functionality post-disruption.

Sound Level Measurement

Sound level measurement assesses environmental noise levels for compliance and safety standards.

UV Intensity Test

UV intensity test assesses the strength of ultraviolet radiation for various applications and compliance standards.

Humidity Mapping

Humidity studies