Filtriraj po Last updated date SelectPoznejePredFrom - To Date Končni datum 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 Rezultati (3838) Sort by Last update date (new to old)Last update date (old to new)A-ZZ-A Leave this field blank European Medicines Agency website on suspected side effect reports now in all 23 EU official languages 18 Junij 2012NewsCorporateMedicines Committee for Medicinal Products for Veterinary Use (CVMP) meeting of 12-14 June 2012 15 Junij 2012Press releaseVeterinary European Medicines Agency finalises guidance on medicines containing monoclonal antibodies 15 Junij 2012NewsHumanMedicines Management Board completes framework for conflicts of interests 8 Junij 2012Press releaseCorporate European Medicines Agency welcomes 1000th orphan designation 7 Junij 2012NewsCorporateMedicines European Medicines Agency launches new electronic form for submission of plasma-master-file applications 7 Junij 2012NewsCorporateMedicines Annual report 2011 shows continuously high level of activities 6 Junij 2012NewsCorporate Revised guideline on quality of biosimilar medicines open for comments 31 Maj 2012NewsHumanBiosimilarsRegulatory and procedural guidance European Medicines Agency boosts EU transparency with online publication of suspected side effect reports 31 Maj 2012Press releaseCorporateMedicines Meeting highlights from the Committee for Medicinal Products for Human Use (CHMP) 21-24 May 2012 25 Maj 2012NewsHuman 1 … 251 252 253 254 255 Page 255 of 384 256 257 258 259 … 384
European Medicines Agency website on suspected side effect reports now in all 23 EU official languages 18 Junij 2012NewsCorporateMedicines
Committee for Medicinal Products for Veterinary Use (CVMP) meeting of 12-14 June 2012 15 Junij 2012Press releaseVeterinary
European Medicines Agency finalises guidance on medicines containing monoclonal antibodies 15 Junij 2012NewsHumanMedicines
European Medicines Agency launches new electronic form for submission of plasma-master-file applications 7 Junij 2012NewsCorporateMedicines
Revised guideline on quality of biosimilar medicines open for comments 31 Maj 2012NewsHumanBiosimilarsRegulatory and procedural guidance
European Medicines Agency boosts EU transparency with online publication of suspected side effect reports 31 Maj 2012Press releaseCorporateMedicines
Meeting highlights from the Committee for Medicinal Products for Human Use (CHMP) 21-24 May 2012 25 Maj 2012NewsHuman