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 (3839) Sort by Last update date (new to old)Last update date (old to new)A-ZZ-A Leave this field blank European Medicines Agency recommends approval of new medicine for Cushing's disease 20 Januar 2012Press releaseHumanMedicines Meeting highlights from the Committee for Medicinal Products for Human Use (CHMP) 16-19 January 2012 20 Januar 2012NewsHumanMedicines European Medicines Agency releases guideline on biosimilar interferon beta for public consultation 20 Januar 2012NewsHumanBiosimilarsRegulatory and procedural guidanceMedicines European Medicines Agency starts review of Gilenya (fingolimod) 20 Januar 2012Press releaseHumanMedicines Committee for Orphan Medicinal Products (COMP) January 2012 highlights 16 Januar 2012NewsHumanRare diseases Committee for Medicinal Products for Veterinary Use (CVMP) meeting of 10-12 January 2012 13 Januar 2012Press releaseVeterinary Public consultation opens on the revised guideline on the evaluation of human anticancer medicines 11 Januar 2012NewsHumanRegulatory and procedural guidance European Medicines Agency starts review of aliskiren-containing medicines following termination of ALTITUDE study 22 December 2011Press releaseHumanMedicines New measures to facilitate conduct of ENCePP studies 22 December 2011News Committee on Herbal Medicinal Products approves four-year work programme 22 December 2011NewsHerbal 1 … 261 262 263 264 265 Page 265 of 384 266 267 268 269 … 384
European Medicines Agency recommends approval of new medicine for Cushing's disease 20 Januar 2012Press releaseHumanMedicines
Meeting highlights from the Committee for Medicinal Products for Human Use (CHMP) 16-19 January 2012 20 Januar 2012NewsHumanMedicines
European Medicines Agency releases guideline on biosimilar interferon beta for public consultation 20 Januar 2012NewsHumanBiosimilarsRegulatory and procedural guidanceMedicines
European Medicines Agency starts review of Gilenya (fingolimod) 20 Januar 2012Press releaseHumanMedicines
Committee for Orphan Medicinal Products (COMP) January 2012 highlights 16 Januar 2012NewsHumanRare diseases
Committee for Medicinal Products for Veterinary Use (CVMP) meeting of 10-12 January 2012 13 Januar 2012Press releaseVeterinary
Public consultation opens on the revised guideline on the evaluation of human anticancer medicines 11 Januar 2012NewsHumanRegulatory and procedural guidance
European Medicines Agency starts review of aliskiren-containing medicines following termination of ALTITUDE study 22 December 2011Press releaseHumanMedicines