Validation
Analytical validation for sequencing is not one experiment. It is five parameters, each with its own sample requirement, and the reference material is usually the constraint.
| 5+ min read
The technology isn’t new. What’s changed is the math behind keeping it manual
Updated | 4 min read
As pharmaceutical analytical workflows grow more demanding, labs are under increasing pressure to balance trace-level accuracy, validation requirements, documentation, and faster development timelines
| 5 min read
How thermal process authority studies, F0 calculations, and scheduled process documentation keep canned food retort operations compliant and safe
| 5+ min read
Biological indicators provide the only direct evidence that an autoclave cycle has achieved the conditions required to kill resistant bacterial spores
| 5+ min read
New actions from the EPA and European Commission signal continued support for non-animal approaches to evaluating chemical hazards
| 2 min read
How lab autoclaves use steam, pressure, and heat to achieve sterility, and what validation and operational practices keep every cycle compliant
| 5+ min read
The Wiley Registry of Mass Spectral Data 2026 grows by 42,000 new GC-MS spectra. Here's what that means for labs running automated identification pipelines
| 5 min read
