Honeywell Product Quality Review Automates and Simplifies Compliance Processes For Manufacturers Of Medical Products

Honeywell launched Honeywell Product Quality Review, a software solution for manufacturers of medical products. The solution is designed to automate and streamline the Annual Product Quality Review (APQR) process, enabling medical organizations to efficiently assess the quality of their products and more efficiently meet regulatory requirements.

Honeywell Product Quality Review is the first of a series of applications in the new Honeywell Life Sciences Applications Suite, each designed to enable rapid digital capabilities and drive business outcomes at scale to improve product quality and patient safety. It replaces paper-based processes, automating data collection from various systems of record, saving valuable time and improving data integrity. 

Under FDA and other global regulatory guidelines, pharmaceutical companies are required to review and assess the quality of their medical products annually. Inefficient APQR programs can result in a time-consuming process of collecting the data from multiple systems and sites and then conducting a manual review, analysis and approval, months after initiating data collection. Poor APQR practices can potentially present unnecessary risks to patients and regulatory actions.