Precision and accuracy of measured values are an essential factor for patient safety. They are the very basis for a safe and reproducible manufacturing, testing and release of excipients, active pharmaceutical ingredients and finished drug products.
Today the continuously progressing process automation is accompanied by large number of measuring and sensor technologies. This is why calibration gains more and more relevance.
We will be happy to support You in setting up and commissioning of a risk-based, GMP-conforming and efficient calibration system.
- Risk analysis according ICH Q9 (EU GMP guidelines part III) for identification and definition of required calibration activities
- Conceptioning and set-up of efficient calibration systems
- Planning and performance of calibration as required during qualification activities
- Planning and performance of re-calibration in accordance with international standards
- Full-service calibration