Production deviations and investigation of quality events, along with the volume of data that must be reviewed and resolved make the process of batch record review and product disposition increasingly complex. TrackWise Digital® and TrackWise AI harness the power of operational data from the shop floor by applying advanced technologies such as the Industrial Internet of Things (IIoT) connectivity to enable rapid decisions and faster product disposition.
DEVIATIONS AND QUALITY EVENTS
Deviations handled in a centralized location, along with associated investigations, approvals, and resulting records
About Deviation Management
Learn about deviation management and quality events, and learn how TrackWise Digital QMS and the TrackWise AI platform fosters collaborative engagement along with the concept of related processes through parent/child relationships.
WHITE PAPER
Enabling Quality by Design
Learn how the integration of Honeywell Experion and TrackWise Digital are increasing the value of QbD.
Blog
Integration of Quality Management and Manufacturing Automation Systems
Integrated quality and batch operations that give organizations real-time, end-to-end visibility, enable faster and better decision making and proactive response to quality events.
Podcast
Patient-Centric Passion: Meet Dr. Oxana K. Pickeral
“It’s not just making sure that you’ve got the right pill of the right color and the right bottle, it’s safety and efficacy and reliability of supply.”
Why Is Deviation Management Important?
- SUPPORTS EFFECTIVE QUALITY MANAGEMENT
- CULTIVATES CONTINUOUS IMPROVEMENT
- SATISFIES REGULATORY COMPLIANCE
- BUILDS TRUST WITH CUSTOMERS
- CONTRIBUTES TO LONG-TERM SUCCESS
What are the Risks of Mismanaging Deviations?
The risks associated with poor deviation management can include:
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RELEASE OF PRODUCTS OR SERVICES THAT ARE SUBPAR OR NOT UP TO COMPANY STANDARDS
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INCREASED COSTS DUE TO THE NEED TO REWORK OR REPLACE DEFECTIVE MATERIALS OR PRODUCTS
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POTENTIAL FOR NONCOMPLIANCE WITH INDUSTRY REGULATIONS AND STANDARDS
Implementing deviations management software can help you address these challenges. By centralizing and automating the deviations management process, software solutions can improve efficiency, reduce errors, and streamline workflows. Deviations management software can also provide real-time visibility into deviation status, progress, and results, making it easier for quality managers to track progress and ensure compliance.
For example, a quality manager in the pharmaceutical industry may be struggling to manage deviations related to the manufacturing process, including deviations related to batch production or equipment malfunction. Deviations management software could help them streamline the process, ensure that all deviations are adequately documented, investigated, and resolved, and track the implementation of corrective and preventive actions to reduce the likelihood of similar deviations occurring in the future.
Similarly, a quality manager in the medical device industry may use deviations management software to manage deviations related to product design or labeling, ensuring that all deviations are appropriately documented, investigated, and resolved, and that the implementation of corrective and preventive actions is adequately tracked and verified. By implementing deviations management software, quality managers can improve compliance, reduce the risk of errors, and demonstrate their organization’s commitment to quality and safety.
Benefits of Using Technology for Deviation Management
Quality management systems can help organizations manage deviations by providing tools and functionality to identify and report deviations, investigate root causes, implement corrective and preventive actions and monitor the effectiveness of those actions. A QMS can also provide visibility into the status of deviation activities, enabling organizations to make informed, data-driven decisions to reduce risk and improve quality.