Social Media Ideas for Good Laboratory Practice

Molecular Devices Expands SoftMax® Pro GxP Software Suite with GLP Mode to Help Laboratories Advance Confidently from D...

New microplate reader software helps laboratories apply appropriate controls as workflows evolve from discovery toward more regulated environments SAN JOSE, Calif., Sept. 17, 2026...

PETcore Europe, KÖR Launch Initiative to Harmonize PET Food Contact Materials Safety Testing

GeNi is intended to serve as a centralized hub for interlaboratory data, enabling participants to benchmark testing performance, identify best practices, improve data comparability...

The Cost of Rework Starts in the Lab, not on the Production Floor

When test results are generated using inconsistent methods or non-standardized procedures, the results do not confidently reflect the true properties of your products.

This is a complete laboratory safety poster. It breaks lab safety into 8 pillars - what to wear, how to behave, and what...

В This is a complete laboratory safety poster. It breaks lab safety into 8 pillars - what to wear, how to behave, and what to do with chemicals, equipment, biological materials, wa...

EPA Seeks Input on Potentially Important Changes to “SW-846” Waste Sampling and Testing Methods

Labs seek standardised testing protocol for FoPL

As the Supreme Court of India scrutinises the Food Safety and Standards Authority of India FSSAI over its proposed Front of Pack Labelling FOPL regime the ongoing litigation has pr...

<![CDATA[6 Ways Lab Data Can Improve Clinical Trials]]>

<![CDATA[Laboratory Advantage: End-to-End Solutions for Increased Complexity in Clinical Trials]]>

Altruist Biologics’ Suzhou Site Receives EMA GMP Certification

The company’s Quality Risk Management framework enabled proactive identification of compliance risks, reduced uncertainties associated with cross-regional technology transfer, and...

Lexogen Expands NGS Services with GCLP-Compliant Workflows

Lexogen’s GCLP-compliant RNA sequencing workflows support clinical research with controlled sample handling, documented processing, data integrity, bioinformatics, reporting, and t...

Beyond Animal Testing: FDA's 2026 Framework for Fit-for-Purpose NAMs

In September 2026, FDA took another significant step toward integrating new approach methodologies, or NAMs, into drug development by issuing a Direct Final Rule on Nonclinical Tes...

Industry Best Practices for Metrology Systems and Metrology Software Validation in FDA-Regulated Environments

As devices become more advanced, manufacturers often need quality control processes that are well documented, repeatable, and aligned with their internal quality systems.