Guidance on Clinical Decision Support (CDS) Software: Industry Impact

Date of Publication: 29-Jan-2026 INTELLIGENCE OVERVIEW Agency: US FDA Regulatory authorities have issued updated guidance on Clinical Decision Support (CDS) software, clarifying how such tools are regulated when used to support healthcare…

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EMA Reflection Paper on Non-Mutagenic Impurities: Industry Impact

Date of Publication: 02-02-2026 INTELLIGENCE OVERVIEW Agency: European Medicines Agency (EMA) The European Medicines Agency (EMA) has published a reflection paper on the qualification of non-mutagenic impurities, providing scientific guidance on…

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EMA Draft Reflection Paper on Qualification of Non-Mutagenic Impurities: Industry Impact

Date of Publication: 30-01-2026 INTELLIGENCE OVERVIEW Agency: European Medicines Agency (EMA) The European Medicines Agency (EMA) has released a draft reflection paper outlining scientific principles for the qualification and control of…

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EMA Type II Variation Checklist: Industry Impact

INTELLIGENCE OVERVIEW The European Medicines Agency (EMA) has issued a Validation Checklist for Type II (non)clinical variations, defining the mandatory documentation required for successful validation of post-authorisation variation applications. Date…

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EMA Recommends Approval of New Sanofi Medicine for Chronic Graft-Versus-Host Disease

INTELLIGENCE OVERVIEW Agency: European Medicines Agency (EMA)Product: Sanofi – New medicinal productIndication: Chronic graft-versus-host disease (cGVHD)Procedure: CentralisedStatus: Positive CHMP opinion Date of Publication: 30-Jan-2026 The EMA’s Committee for Medicinal Products…

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Strengthening Data Transparency & Regulatory Harmonisation in Europe

Agency/Company: European Medicines AgencyCountry: European UnionDate: 22-Jan-2026 Intelligence Overview: The European Medicines Agency’s guidance on the Product Management Service (PMS) highlights a major step forward in implementing ISO IDMP standards…

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