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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Japan Updates JPMA Self-Inspection Checklist for Qualit…
On March 26, 2026, the Japan Pharmaceutical Manufacturers Association (JPMA) published a revised self-inspection checklist for quality tes…
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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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Brazil ANVISA Updates COVID-19 Vaccine Strains, Low-Ris…
On March 24, 2026, the Brazilian National Health Surveillance Agency (ANVISA) announced a set of regulatory updates impacting COVID-19 vacci…
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Türkiye Updates Packaging and Patient Leaflet Rules fo…
The Turkish Medicines and Medical Devices Agency published substantial revisions to its guideline on package information and patient informa…
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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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FDA Launches Unified Adverse Event Monitoring System (A…
On March 11, 2026, the U.S. Food and Drug Administration (FDA) launched the Adverse Event Monitoring System (AEMS), a unified platform desig…
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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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