Autoscribe LIMS Blog

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Regulatory

How LIMS Ensures FDA 21 CFR Part 11 Compliance

Regulated laboratories need to ensure electronic records and electronic signatures can be relied upon in the same way as paper records and hand written signatures. Using a LIMS helps enforce signature policies to meet FDA 21 CFR Part 11.

24th April 2024

What’s Important When Selecting a LIMS?

When selecting a laboratory information management system (LIMS), whether it’s your first or you’re replacing an existing solution, the temptation is to concentrate solely on your user requirements. It really does make sense to document these and match them to the features of potential LIMS products.

2nd April 2024

Regulatory

The Clock Ticks for US Food Testing Labs to be LAAF-Accredited

FDA is gradually tightening the rules on food testing labs to mandate that, under certain circumstances, food testing must be performed only by LAAF-accredited laboratories. This article discusses how this affects contract testing labs and how the can comply with the amendments to Food Safety Modernization Act.

13th March 2024

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