Industry Solutions

Quality Management System

Chemicals manufacturers must follow Good Manufacturing Practices (GMP), ISO requirements, customer quality expectations, and other standards. The ability to log, manage and report on quality management-related information is a key requirement in meeting industry best practices and regulatory requirements. In addition, chemical manufacturers must proactively identify trends and indicators for out of specifications (OOS).

In addition to regulatory challenges, the chemical industry faces increased competition and rising production costs leading to further pressure for cost containment. Using paper-based forms, disconnected systems, or manual processes to manage, track and report on quality related issues are inefficient and costly, and do not provide the control required to minimize the risk.

TrackWise Enterprise Process Management Software

Leading companies have turned to TrackWise as their enterprise quality management software solution to reduce risk and streamline quality and safety management processes in their organizations. TrackWise improves efficiency, reduces costs, and increases profitability by centralizing and integrating all quality processes, including management and reporting of deviations, customer complaints, supplier quality, internal and external audits, change control, corrective and preventive actions (CAPA), preventive maintenance and calibration, training management, document management and others.

TrackWise provides the unique capability to manage all issues, actions, and changes in a centralized and integrated system. Automated workflow and configurable business rules ensure processes are followed, while enterprise reporting provides reliable information upon request to support decision-making and improve cycle times.

TrackWise enables you to

  • Comply with GMP, OSHA, EPA, ISO, and other quality and safety requirements.
  • Implement an effective and closed-loop quality management system.
  • Manage, track, and report on deviations, investigations, corrective actions, and other actions required when requirements are not met.
  • Reduce risk by eradicating any potential of missing records, missing data, or missed approvals.
  • Shorten product release cycle time by closing corrective and preventive actions faster.
  • Increase visibility by alerting users when work is required and automatically escalating late issues.
  • Eliminate errors and repeat problems by automating workflow.
  • Exceed industry standards for employee and supervisor training on proper safety procedures.
  • Improve enterprise reporting with easy-to-use search tools and powerful reporting features.