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MedicineHumanAuthorised
MedicineHumanAuthorised
MedicineHumanAuthorised
MedicineHumanAuthorised
MedicineHumanAuthorised

EMA's Good Manufacturing Practice (GMP) / Good Distribution Practice (GDP) Inspectors Working Group is organising a two-day workshop to help shape a risk-based approach to the use of generative artificial intelligence (AI) in medicines manufacturing.

EventHumanCompliance and inspectionsRegulatory and procedural guidanceResearch and development

The Clinical Trials Information System (CTIS) Info Day provides a comprehensive update on the CTIS, including progress made, upcoming priorities, and key legal and regulatory developments affecting CTIS.

EventHumanCorporateClinical trials
PIPHuman
PIPHuman
PIPHuman