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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FDA, MHRA, and Health Canada Announce Joint Symposium o…
On March 10, 2026, the U.S. Food and Drug Administration (FDA), in collaboration with the Medicines and Healthcare products Regulatory Agenc…
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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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U.S. FDA Introduces AEMS: A Unified Platform for Advers…
On 11 March 2026, the U.S. Food and Drug Administration (FDA) introduced theAdverse Event Monitoring System (AEMS), a centralized platform…
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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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New Zealand MPI Issues Food Export Compliance Guidance …
On March 13, 2026, the Ministry for Primary Industries (MPI) in New Zealand released new guidance outlining compliance expectations for expo…
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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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EMA Opens Applications for 2026 Portfolio and Technolog…
On March 10, 2026, the European Medicines Agency (EMA) announced that applications are now open for Portfolio and Technology Meetings (P…
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