ISO/IEC 17025:2017 is an international standard for testing and calibration laboratories to ensure adherence to a set of uniformed procedures primarily for third-party calibration services. It outlines requirements for a quality management system (QMS) and technical competence, ensuring the production of precise and accurate test and calibration data. As an ISO 17025:2017 compliant laboratory, Bio-Pharma Calibration demonstrates our commitment to excellence, technical proficiency, and a rigorous approach to quality.
Compliance with ISO 17025:2017 is becoming increasingly critical as the FDA and other regulatory agencies worldwide are intensifying requirements for accurate and reliable testing and calibration services. This adherence not only showcases our technical capabilities but also instills confidence in our clients, knowing their partners operate under the most stringent quality standards. It is a testament to our dedication to quality, continuous improvement, and customer satisfaction.