UK FSA Clarifies Evidence Requirements for Precision Fe…
On March 20, 2026, the Food Standards Agency (FSA) published supplementary guidance for novel food applications involving products deri…
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EU Regulation Expands List of Animal-Origin Products Su…
On March 16, 2026, the European Commission published a new regulation updating official control requirements for products of animal origin, …
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UK MHRA Sets Regulatory Pathway to Phase Out Animal Tes…
On March 24, 2026, the Medicines & Healthcare products Regulatory Agency (MHRA) introduced new regulatory principles for human medicines…
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EU PFAS Restrictions: ECHA Launches SEAC Consultation w…
On March 26, 2026, the European Chemicals Agency (ECHA) launched a public consultation on a draft opinion issued by the Committee for Socio-…
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Netherlands MEB Introduces Declaration Requirement for …
On March 11, 2026, the Medicines Evaluation Board (MEB) in the Netherlands published new declaration guidance for applicants seeking Duplex …
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MHRA and NICE Launch Aligned Licensing and HTA Process …
On March 17, 2026, the Medicines and Healthcare products Regulatory Agency (MHRA) and the National Institute for Health and Care Excellence …
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ECHA Advances Draft SEAC Opinion on EU-Wide PFAS Restri…
On March 11, 2026, the European Chemicals Agency (ECHA) announced a draft opinion from its Committee for Socio-Economic Analysis (SEAC) rega…
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UK Updates Novel Foods Authorisation Guidance: Key Chan…
On March 12, 2026, the Food Standards Agency (FSA) and Food Standards Scotland (FSS) published updated guidance on the authorisation process…
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Spain Approves New Regulation to Streamline Geographica…
On March 10, 2026, the Spanish Ministry of Agriculture, Fishing and Nutrition (MAPA) announced that the Spanish Council of Ministers approve…
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Greece’s EOF Reopens Platform for Authenticity Tape D…
On March 9, 2026, the National Organization for Medicines announced the temporary reopening of its digital submission platform for the dec…
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