Φιλτράρισμα ανά Last updated date SelectΜετάΠρινFrom - To Date Ημερομηνία λήξης This week This month Last week Last month Category HumanCorporateVeterinaryHerbal Topic MedicinesCOVID-19PharmacovigilanceVaccinesReferralsPaediatricsRare diseasesRegulatory and procedural guidanceClinical trialsAdvanced therapiesData on medicinesCompliance and inspectionsInnovationMedicine shortagesResearch and developmentBiosimilarsSMEAntimicrobial resistanceCorporateGovernanceBrexitQuality of medicinesGeneric and hybrid medicinesEarly accessMedicines for use outside the EUFeesProduct informationScientific adviceMedical devicesMaximum residue limitMpoxBiologicalsScientific guidelinesVeterinary limited marketsCompassionate usePRIMECareersMedication errorParallel distributionProcurement Diseases area Viral diseasesCancerImmune-system diseasesDiabetesNeurodegenerative diseasesCardiovascular diseasesHIV and AIDS Responsible body CHMP CVMP PRAC Management Board COMP PDCO CMDh HMPC CAT Patient safety information Patient safety Leave this field blank Filter Αποτελέσματα (3838) Sort by Last update date (new to old)Last update date (old to new)A-ZZ-A Leave this field blank Closer ties on medicines safety between European and Canadian regulatory authorities 11 Ιανουάριος 2008Press release Meeting highlights from the Paediatric Committee: 18 - 20 December 2007 10 Ιανουάριος 2008Press releaseHumanPaediatrics European Risk Management Strategy: 2008-2009 work programme adopted 20 Δεκέμβριος 2007Press release Committee for medicinal products for veterinary use: Meeting of 11-13 December 2007 14 Δεκέμβριος 2007Press releaseVeterinary European Medicines Agency concludes new advice to doctors and patients for Champix needed 14 Δεκέμβριος 2007Press releaseMedicines Guerbet withdraws its marketing authorisation application for Sinerem 14 Δεκέμβριος 2007Press releaseHuman Meeting highlights from the Committee for Medicinal Products for Human Use,10-13 December 2007 14 Δεκέμβριος 2007Press releaseHuman European Medicines Agency recommends withdrawal of the marketing authorisations for lumiracoxib-containing medicines 13 Δεκέμβριος 2007Press releaseHumanMedicines Meeting highlights from the Paediatric Committee: 21 - 23 November 2007 27 Νοέμβριος 2007Press releaseHumanPaediatrics The European Union and the Food and Drug Administration working together to create common application for orphan designation for Medicines 26 Νοέμβριος 2007Press releaseMedicines 1 … 317 318 319 320 321 Page 321 of 384 322 323 324 325 … 384
Closer ties on medicines safety between European and Canadian regulatory authorities 11 Ιανουάριος 2008Press release
Meeting highlights from the Paediatric Committee: 18 - 20 December 2007 10 Ιανουάριος 2008Press releaseHumanPaediatrics
Committee for medicinal products for veterinary use: Meeting of 11-13 December 2007 14 Δεκέμβριος 2007Press releaseVeterinary
European Medicines Agency concludes new advice to doctors and patients for Champix needed 14 Δεκέμβριος 2007Press releaseMedicines
Guerbet withdraws its marketing authorisation application for Sinerem 14 Δεκέμβριος 2007Press releaseHuman
Meeting highlights from the Committee for Medicinal Products for Human Use,10-13 December 2007 14 Δεκέμβριος 2007Press releaseHuman
European Medicines Agency recommends withdrawal of the marketing authorisations for lumiracoxib-containing medicines 13 Δεκέμβριος 2007Press releaseHumanMedicines
Meeting highlights from the Paediatric Committee: 21 - 23 November 2007 27 Νοέμβριος 2007Press releaseHumanPaediatrics
The European Union and the Food and Drug Administration working together to create common application for orphan designation for Medicines 26 Νοέμβριος 2007Press releaseMedicines