In healthcare manufacturing, cleanliness is not simply a matter of good housekeeping; it is a...
Sample Receipt: Why This First Step Matters in a GMP-Compliant CRO
For a contract research organisation (CRO), the sample receipt area is far more than an administrative handover point. It is the first controlled stage in the laboratory workflow and often the moment where the quality, identity and traceability of a...
Results - 63 Blogs
Extractables and leachables (E&L) assessment has always been a key area of focus for the...
How to plan ahead from March 2026 Health Canada has published Version 4.0 of the Good Manufacturing...
Good Manufacturing Practice (GMP) compliance is fundamental for laboratories operating in regulated...
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~Broughton introduces ISO/IEC 17025-accredited cannabinoid testing for oils and tinctures~
For much of the past decade, the US nicotine and ENDS marketplace has operated in a state of...
In 2025, Sweden achieved something virtually unheard of elsewhere: it became and may soon be...
As the U.S. Food and Drug Administration’s Center for Tobacco Products (CTP) adjusts to a new era...
As the U.S. Food and Drug Administration (FDA) seeks to modernise its regulatory processes,...
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