Blog
- April 27, 2023
As we discussed in an earlier post, the humble signature has become more complicated — and more regulated — with the advent of digital and electronic technologies. Here’s a quick...
- March 3, 2023
When was the last time you had to sign an actual document with ink? For me, it might have been my mortgage ten years ago. Today, we routinely email documents...
- January 14, 2022
Achieving and maintaining accreditation is critical to forensic laboratories. The media is full of examples of what happens when quality work is compromised. Not only can a forensic lab lose...
- June 5, 2019
The emergence of LIMS and other informatics tools have irrevocably changed the way labs manage data. As LIMS’ role has become more prominent, compliance and validation have grown increasingly complex....
- April 30, 2019
What’s a Biobank? Easy – a collection of data and samples. And what is a biobank’s core function? Managing those samples and compiling that data (depending on the biorepository’s focus,...
- September 14, 2018
You might have noticed the flurry of movement in April and May as companies finalized compliance with Europe’s General Data Protection Regulations (GDPR). LabVantage also ensured that the LabVantage LIMS...
- June 15, 2018
In a previous post, we discussed the increasing regulatory focus being placed on Temporary Data. It’s an important topic that has far reaching implications for LIMS (and other) platforms, but...
- January 19, 2017
LabVantage has always used international standards to create and sustain our practices and procedures. We rely upon IEEE for our testing methodology, GAMP for our LabVantage Pharma package, ICH for our risk management...