Prepare for a safe return to work

Increase traceability, safety and security with a digital visitor management system

As vaccination rates increase across the country, we can all see a brighter future ahead. However, the potential for COVID-19 outbreaks certainly still remains and it’s crucial to ensure measures are in place to keep people safe at your premises.

Pitney Bowes offers a contactless, digital solution, LobbyTrac™, providing a compact, secure and safe way to manage employees, contractors and visitors at your sites.

Benefits of Pitney Bowes LobbyTrac include:

  • Quick reporting of who is or has been at your offices to ensure compliance and support contact tracing if needed.
  • ·Automate the COVID vaccination certificates process so you can keep a record of who’s been vaccinated.
  • Ability to customise sign-in to include health and safety questions.
  • Contactless check-in: online pre-registration rather than physical check-in.
  • Automatic notifications of visitor’s arrival to relevant staff member(s).
  • Improved safety and security of staff and visitors.
  • Easy management of contractor access and authorisations.
  • Integration with internal contractor induction workflows.
  • Available in a range of models to suit different business needs and requirements.

Introducing PB TempCheck*
Easily check a person’s temperature upon their arrival with PB TempCheck, an infrared temperature scanning device.

*PB TempCheck is an infrared temperature scanning device, listed on the Australian Register of Therapeutic Goods (ARTG), under reference number 345754 by Stericlick Pty Ltd -Thermometer, infrared, skin. The device is a battery powered infrared thermometer intended for screening people in public places. The thermometer is intended for intermittent measurement and monitoring of human body temperature from the forehead. The device is indicated for people of all ages and suitable for public places. The device is subject to compliance with conditions under Part 4-5, Division 2 of the Therapeutic Goods Act 1989 and Part 5, Division 5.2 of the Therapeutic Goods (Medical Devices) Regulations 2002. ALWAYS READ THE INSTRUCTIONS FOR USE. FOLLOW THE INSTRUCTIONS FOR USE.

To request a demo or learn more, please complete the form below.