How to plan ahead from March 2026 Health Canada has published Version 4.0 of the Good Manufacturing...
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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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,...
Since January 2025, the regulatory landscape for tobacco and nicotine products in the United States...
When developing a nicotine product, the choice between freebase nicotine and nicotine salts plays a...
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