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 Comments invited on draft reflection paper on data requirements for iron-based nanocolloidal products developed with reference to an innovator medicine 7 Oktober 2013NewsHuman European Medicines Agency's Management Board supports plan to publish agendas and minutes of all committees 7 Oktober 2013Press releaseCorporate EU and Japan improve information-sharing in the area of good manufacturing practice using EudraGMDP database 7 Oktober 2013NewsCorporateCompliance and inspections European Medicines Agency begins to publish recommendations based on safety signals 4 Oktober 2013NewsHumanMedicinesPharmacovigilance European Medicines Agency publishes report on conflicts of interests workshop 2 Oktober 2013NewsCorporateMedicines Public consultation on the publication and access to clinical-trial data now closed 1 Oktober 2013NewsCorporate European Medicines Agency publishes a video explaining the concept of medicines under additional monitoring 1 Oktober 2013Press releaseCorporateMedicines European Medicines Agency publishes a video explaining the concept of medicines under additional monitoring 1 Oktober 2013Press releaseCorporateMedicines Consultation on updated guideline on clinical development of medicines for treatment of HIV infection 30 September 2013NewsCorporateRegulatory and procedural guidance World Heart Day – more guidance for medicines developers 27 September 2013NewsCorporate 1 … 217 218 219 220 221 Page 221 of 384 222 223 224 225 … 384
Comments invited on draft reflection paper on data requirements for iron-based nanocolloidal products developed with reference to an innovator medicine 7 Oktober 2013NewsHuman
European Medicines Agency's Management Board supports plan to publish agendas and minutes of all committees 7 Oktober 2013Press releaseCorporate
EU and Japan improve information-sharing in the area of good manufacturing practice using EudraGMDP database 7 Oktober 2013NewsCorporateCompliance and inspections
European Medicines Agency begins to publish recommendations based on safety signals 4 Oktober 2013NewsHumanMedicinesPharmacovigilance
European Medicines Agency publishes report on conflicts of interests workshop 2 Oktober 2013NewsCorporateMedicines
Public consultation on the publication and access to clinical-trial data now closed 1 Oktober 2013NewsCorporate
European Medicines Agency publishes a video explaining the concept of medicines under additional monitoring 1 Oktober 2013Press releaseCorporateMedicines
European Medicines Agency publishes a video explaining the concept of medicines under additional monitoring 1 Oktober 2013Press releaseCorporateMedicines
Consultation on updated guideline on clinical development of medicines for treatment of HIV infection 30 September 2013NewsCorporateRegulatory and procedural guidance