Modernized Approach to APQR Process
Honeywell Product Quality Review (HPQR) offers a cutting-edge solution to annual product quality review (APQR) requirements essential for drug product manufacturers. By digitizing the process, HPQR simplifies APQR reports' creation, starting from sourcing data to generating a comprehensive final report. This streamlined approach enhances operational efficiency and ensures compliance with Good Manufacturing Practice (GMP) regulations.
Enhanced Productivity and Accuracy
Through automated data collection and approval workflows, HPQR significantly improves productivity and accuracy in product quality reviews. The platform enables proactive assessments with virtual or interim product quality reviews and conducts complex statistical analyses automatically. By meeting regulatory standards like 21 CFR Part 11, HPQR ensures high-quality products while reducing manual work and errors.
Collaborative Review Process
One of the key features of HPQR is its focus on cross-functional collaboration. Users can easily track assigned tasks, invite contributions from various departments, and collaborate seamlessly on product quality reviews. The platform allows for streamlined approvals, email notifications, digital signatures, and the ability to incorporate comments for continuous improvement based on feedback received.
Resources for Continuous Improvement
Honeywell provides valuable resources to optimize the APQR process and enhance product quality. Accessing whitepapers, datasheets, and partnering with experienced providers empowers organizations to streamline operations, enhance product quality, and stay ahead of industry standards. By joining the Honeywell community, companies can benefit from the latest news, insights, and best practices in the life sciences sector.