MadgeTech Blog

What is 21 CFR Part 11?

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In 1997, the Food and Drug Administration (FDA) issued Part 11 of Title 21 defining the criteria under which electronic records and signatures are considered equivalent to paper records and handwritten signatures. As much controversy and confusion this regulation has caused over the years, it will actually make your life easier and clutter-free by creating a compliant and paperless quality management system.

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MadgeTech Raising the Bar on Data Acquisition with Advancements to the Titan S8

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You asked, we listened. MadgeTech’s 8-channel, touchscreen data acquisition logger, the Titan S8, is now equipped with wireless capabilities! All you need is a Wi-Fi network or Ethernet to transform this powerful device into a streamlined monitoring solution.

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