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Many companies certified to ISO 9001 struggle with ISO 13485. Learn why risk management, documentation, supplier controls, and regulatory requirements demand a fundamentally different approach for medical device manufacturers.

Alaska’s newly authorized hazardous waste program introduces state-specific requirements. Learn what this regulatory change means for RCRA compliance teams managing operations within Alaska.

Discover how wildfires and pollution may impact produce safety.

In this article, we explore why phase I clinical trial submissions in Belgium may trigger FAMHP RFIs, and how clearer protocol and investigator’s brochure reasoning can help sponsors prepare before filing.

The UK plans to revise the GB MCL list of hazardous substances and mixtures.

Learn how operational readiness helps developers and operators ensure customer confidence and accelerate the move to revenue-generating operations.

Investment in Saint-Benoît expands bioanalytical capabilities, supporting larger studies and accelerating drug development globally.

Learn how biostatistics supports IDMC review with validated outputs, patient-level context, live data clarification and controlled handling of unblinded trial data.

Montenegro mandates compliance documentation for food contact ceramics while maintaining existing lead and cadmium limits.

China published GB/T 29862-2026, introducing updated textile fiber content labeling requirements, effective August 1, 2027.