Minimize future internal defects and deviations.

Detecting internal defects and deviations is a basic parameter for optimizing the work processes of your company. Effective management and root-cause investigation mean that in the future you will be able to avoid the majority of them, reduce waste, and thus maximize your company’s profits.

This module contains the following functions:

  • Easy registration of internal defects and deviations from both PC, tablet and mobile devices
  • Lists of open and closed defects and deviation cases
    – both with a quick search, column customization, grouping, and detailed search. You can save your customized lists for later use
    – all lists can be exported to Excel, CSV, or XML
  • Case card with defect type, order numbers, problem description, here-and-now solution, root-cause investigation, risk analysis for repetition, preventive actions, images, documents and immediate creation of improvement proposals if necessary
  • Export of Excel defect/deviation report
  • Assignment of responsible case manager
  • Tracking the processing time of the case
  • Drill-down diagrams for rapid analysis of internal defects and deviations for the effective minimization of similar cases in the future

Get a 4-week free demo account

Wismatix QMS is an online quality management system (eQMS) available on your favorite platform through your preferred web browser. The system is fast and easy to use on a daily basis, and you get access to a very efficient analytical tool that helps you get the most out of your registration and improvement efforts.

Wismatix QMS contains all the features you need to run your management system as efficiently as possible.

The system supports multiple standards within quality management, environment management, food safety, IT security, and medical devices, e.g.:

  • Quality management standards and regulations – ISO 9001, ISO 13485, MDSAP hereunder FDA 21 CFR Part 820
  • Environmental management standards – ISO 14001, ISO 45001
  • IT security management standards ISO 27001, FDA Title 21 CFR Part 11

Get your own hands-on experience with a FREE Demo account. – If you’re serious about simplifying and boosting your Quality Management System, then go ahead and sign up now, no strings attached!

With a free demo account, you can get your own hands-on experience in our sandbox environment for a whole 4-week period.

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