FDA Draft Guidance on Responding to Form 483 Observations After Drug CGMP Inspections

Date of Publication: 03-Mar-2026 INTELLIGENCE OVERVIEWAgency: USFDAThe U.S. Food and Drug Administration (FDA) has released a draft guidance titled “Responding to FDA Form 483 Observations at the Conclusion of a…

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EMA Releases Draft Guidance on Conducting Clinical Trials During Public Health Emergencies

Date of Publication: 04-Mar-2026 INTELLIGENCE OVERVIEWAgency: EMAThe European Medicines Agency (EMA) has released a draft guidance on the conduct of clinical trials during public health emergencies, published on 27 February…

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HSA Updates SG-HSA eCTD Specification for Module 1 and Regional Information (v1.1)

Date of Publication: 04-Mar-2026 INTELLIGENCE OVERVIEWAgency: Health Sciences Authority - SingaporeThe Health Sciences Authority (HSA), Singapore has released an updated guidance document titled “SG-HSA eCTD Specification and Guidance for Use…

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EMA Concept Paper on Microbiome-Based Medicinal Products: Regulatory Direction for Non-Clinical Development

Date of Publication: 02-Mar-2026 INTELLIGENCE OVERVIEWAgency: EMAThe European Medicines Agency (EMA), through its Committee for Medicinal Products for Human Use (CHMP), adopted a draft concept paper (EMA/CHMP/30023/2026) for public consultation…

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Meeting highlights from the Committee for Medicinal Products for Human Use (CHMP) 23-26 February 2026

Date of Publication: 27-Feb-2026 INTELLIGENCE OVERVIEW:Agency: EMAThe European Medicines Agency (EMA) has published its latest Committee for Medicinal Products for Human Use (CHMP) meeting highlights, detailing positive opinions and key…

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EMA Recommends New Single-Dose Oral Treatment: A Major Step Forward in Global Health

Date of Publication: 27-Feb-2026 INTELLIGENCE OVERVIEWAgency: EMAApplicant: Sanofi Winthrop IndustrieProduct: Acoziborole WinthropThe European Medicines Agency (EMA) has highlighted a significant advancement with its update on a new single-dose oral treatment.…

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EMA Reference Documents for Electronic Reporting to EudraVigilance

Date of Publication: 23-Feb-2026 INTELLIGENCE OVERVIEWAgency: EMAThe European Medicines Agency (EMA) has published an updated list of reference documents supporting electronic safety reporting to the EudraVigilance system. This resource outlines…

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EMA Releases Draft Guideline on Quality Aspects of mRNA Vaccines for Veterinary Use

Date of Publication: 20-Feb-2026 INTELLIGENCE OVERVIEWAgency: EMAThe European Medicines Agency (EMA), through its Committee for Veterinary Medicinal Products (CVMP), has released a draft guideline outlining the quality requirements for mRNA…

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EMA Revises Guideline on Risk Management Requirements for Elemental Impurities in Veterinary Medicinal Products (Revision 3)

Date of Publication: 20-Feb-2026 INTELLIGENCE OVERVIEWAgency: EMAThe European Medicines Agency (EMA) has released Revision 3 of its guideline on risk management requirements for elemental impurities in veterinary medicinal products. This…

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EMA Pharmacovigilance Recommendations for Centrally Authorised Veterinary Medicines – 2026

Date of Publication: 19-Feb-2026 INTELLIGENCE OVERVIEWAgency: EMAThe European Medicines Agency (EMA) has published its updated pharmacovigilance-related regulatory recommendations for centrally authorised veterinary medicinal products during 2026. The document provides outcomes…

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