For most pharmaceutical and regulated environments, we recommend a full calibration every 6 to 12 months, depending on your SOPs and instrument usage. However, critical instruments in high-throughput labs may require quarterly verification to ensure zero deviations during audits.

Yes. We provide comprehensive Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) protocols. Our documentation is designed to meet USP/BP and ISO 17025 standards, ensuring your equipment is audit-ready from day one.

Our PM service for pharma machinery (like tablet presses or granulators) includes a full electronic diagnostic, mechanical alignment, lubrication, and wear-part replacement. We focus on identifying potential failure points before they cause expensive production downtime.

Yes. For heavy machinery such as tablet presses, coating pans, and industrial mixers, our engineering team performs on-site calibration and validation. This minimizes the risk associated with moving sensitive equipment and ensures that the machinery is calibrated within its actual operating environment.