Since December, FDA actions have begun to define a more targeted and consequential regulatory...
The Evolving Regulatory Expectations for Extractables and Leachables
Extractables and leachables (E&L) assessment has always been a key area of focus for the pharmaceutical and food sectors in order to ensure that there is no inadvertent toxicity related to packaging. However, for medical devices and nicotine...
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How to plan ahead from March 2026 Health Canada has published Version 4.0 of the Good Manufacturing...
The World Nicotine Congress (WNC) brought together global leaders from science, industry,...
A key focus in discussions around the safety of nicotine pouches relates to child-resistant...
In today’s highly regulated laboratory environment, generating data is no longer enough. GMP...
Good Manufacturing Practice (GMP) compliance is fundamental for laboratories operating in regulated...
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The inaugural York and North Yorkshire Life Sciences Forum was opened by Geoff Davison, CEO of...
In a regulated environment, quality is often described in terms of systems, procedures, and...
On February 10, 2026, FDA’s Center for Tobacco Productsconvened a full-day Small Manufacturer ENDS...
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