Quality Management
21 CFR Part 11 mandates the use of certain lab software features, but labs in unregulated environments can benefit from them as well
| 2 min read
Here are seven tips for AI to help you harness it in your lab—while protecting your data and ensuring reproducible results
Updated | 2 min read
While FDA guidelines demand both technical and procedural controls for lab software compliance, there are some steps lab managers can take to make the most informed purchasing decision
Updated | 3 min read
Carlee McClintock, PhD, shares strategies for lab leaders to move beyond compliance and build a culture of trust, accountability, and continuous improvement
| 3 min read
Agility, collaboration, and innovation keep environmental testing labs ahead of the curve
| 3 min read
Optimize pharma analytical data management & archiving with LIMS. Ensure compliance, integrity, and efficiency in your lab workflows. Get actionable strategies now!
| 5+ min read
FAIR Principles are reshaping information management in clinical labs. Here’s what lab managers need to know to make FAIR work for them
| 4 min read
One unlogged balance adjustment can corrupt an otherwise clean audit trail
| 1 min read
Ensure that the electronic data systems contribute to the trust and reputation of the lab
| 3 min read
Validated methods and technologies help labs meet regulatory expectations and address technical challenges in PFAS analysis and beyond
| 1 min read
Transitioning to GMP production? Learn how to prevent equipment setbacks, build manufacturer partnerships, and foster a strong compliance culture
| 4 min read
A practical guide to strengthening your quality system, reducing repeated nonconformances, and creating a proactive, solution-focused culture
| 5 min read
