Articles and in-depth guides on LIMS, lab automation, and lab regulations
QBench won the LIMS Momentum Leader badge for the second quarter in a row in G2’s Fall 2024 Reports and continues to rank #1 on G2’s Highest Rated LIMS in North America list.
Looking to meet ISO 17025 standards in your lab? Here’s a guide to which software platforms will be the biggest help.
Looking to meet GxP standards in your lab? Here’s a guide to which software platforms will be the biggest help.
In the market for a LIMS? Browse the industry winners and see which one is the best LIMS of 2024.
ISO/IEC 17025 is a key standard for labs to meet if they wish to show the accuracy and reliability of their results. Learn what ISO 17025 is, its requirements, and how a LIMS will help your lab meet it.
From business KPIs to compliance, we’re breaking down the top metrics that labs need to track. Get our FREE downloadable guide.
Automation is the most powerful - and most misunderstood - capability of a LIMS. Learn more about how a LIMS can automate your lab.
QBench continues to rank #1 on G2's Top LIMS in North America list and won several Spring 2024 badges from G2.
GxP outlines good practices for labs across industries. In this guide, we’ll outline how your lab can meet GxP requirements with a LIMS.
Data integrity and security are critical to the success of your lab. See how a LIMS can help protect your lab’s data.
Learn the step-by-step process to successfully implement a LIMS in your lab using this guide.
FDA Title 21 CFR Part 11 is a set of regulations established by the FDA that outlines the requirements for electronic records and electronic signatures.
QBench now tops the Highest-Rated LIMS in North America list, ranked in 12 G2 Winter 2024 Reports, and won several G2 Winter 2024 badges.
Sample management is a core competency of any lab, yet many are falling behind with manual processes. Learn how modern labs are using a LIMS to automate their sample management processes.
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