HPQR – Honeywell Product Quality Review

Modernize the Annual Product Quality Review (APQR) Process

Learn More About HPQR

Introducing HPQR 

The annual product quality review (APQR) process is a requirement for pharmaceutical companies to comply with Good Manufacturing Practice (GMP) regulations and maintain high quality products. However, data aggregation tasks and siloed analysis can hinder product quality decisions, leading to inefficiencies and errors in the APQR process.

 

Streamline the creation of APQR reports with the Honeywell Product Quality Review (HPQR) app. Say goodbye to burdensome manual efforts and embrace a streamlined process that enhances collaboration, improves operational efficiency and meets regulatory compliance. Experience the future of APQR reporting with HPQR. 

 

DOWNLOAD DATASHEET: HPQR

Key Benefits of HPQR

 
 
Improve Efficiency and Data Integrity

HPQR enables users to quickly access and analyze data from multiple systems, reducing manual errors and redundancy. Automating data collection and analysis enhances operational efficiency while maintaining data integrity.

Proactive, Anytime Reviews

With HPQR, users can create virtual or interim PQRs to routinely assess product quality and track continuous improvement initiatives. Simplifying and automating the review process empowers proactive quality management.

Simplify Report Creation and Collaboration

HPQR allows users to automate complex analysis of quality data and collaborate seamlessly across departments. Real-time collaboration ensures swift identification and resolution of product quality issues.

HPQR Features

 
 
Automated Analyses and Report
  • Automatically collect and compile quality data across sites and systems into a centralized report.
  • Generate statistical analyses, standard charts and chapters for product quality reviews and send to stakeholders with a single click.
 
 
Collaboration and Configurable Approval Workflow
  • Initiate the product quality review (PQR) process, assign users, tasks and approvals for seamless collaboration.
  • Never miss a task or an update—get instant notifications on open actions and report status.
 
 
Electronic Signature and Audit Trail
  • PDF reports contain signatures that support compliance with 21 CFR Part 11 regulations.
  • The data, interaction, collaboration and comments within HPQR are all part of the audit trail and adhere to 21 CFR Part 11 compliance.
  • Generate a final APQR in PDF format, ready for submission to the FDA. 

The annual product quality review (APQR) process is a requirement for pharmaceutical companies to comply with Good Manufacturing Practice (GMP) regulations and maintain high-quality products. However, data aggregation tasks and siloed analysis can plague APQR preparation, often hindering product quality decisions and leading to inefficiencies and errors in the process. 
 

Download the white paper to learn how automating the APQR process can help simplify your product quality review process and help you make informed product quality decisions quicker and on a more routine basis.  

  

DOWNLOAD WHITE PAPER

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