Implementing effective temperature calibration in pharmaceutical facilities involves a systematic approach. First, it is essential to identify all temperature-sensitive equipment and establish a calibration schedule based on the manufacturer's recommendations and regulatory requirements. Calibration should be performed using traceable standards by trained personnel or accredited calibration service providers. For instance, when calibrating autoclaves, both temperature and pressure indicators must be assessed to ensure they meet specified tolerances. Detailed records of calibration activities, including dates, results, and corrective actions taken, should be meticulously maintained. Additionally, implementing a robust quality management system that includes regular reviews and audits of calibration procedures will help in identifying areas for improvement and ensuring ongoing compliance with industry standards.