Request demo

Digitize Your Equipment Clean and Use Log for 
Maximum Compliance

We developed our io.Equipment module to enhance your Shiftconnector enterprise platform to help pharmaceutical teams comply with Good Manufacturing Practices (GMP) regulations. Our io.Equipment module is FDA 21 CFR part 11 compliant and provides:

  • electronic signatures
  • multi-level password authentication
  • activity time-stamped with security to your data
  • audit trails to data storage
Activity Stream
Activity Stream

io.Equipment Standardizes Your Logbook Across Teams and Sites Simplified information and documentation solution

Digital recording of data makes information accessible and transparent at all times.

          • Keep track of all events such as production, cleaning, maintenance, breakdowns and calibration of equipment
          • Simplify documentation processes and easily create reports based on your needs
          • Retrrieve data in real-time, 24/7
          • Access research features, e.g. for batch releases or continuous improvement

This website stores cookies on your computer. These cookies are used to collect information about how you interact with our website and allow us to remember you. We use this information in order to improve and customize your browsing experience and for analytics and metrics about our visitors both on this website and other media. To find out more about the cookies we use, see our Privacy Policy

If you decline, your information won’t be tracked when you visit this website. A single cookie will be used in your browser to remember your preference not to be tracked.