Filtrer efter Last updated date SelectEfterFørFrom - To Dato Slutdato Denne uge Denne måned Seneste uge Seneste måned Category HumanCorporateVeterinaryHerbal Topic MedicinesCOVID-19PharmacovigilanceVaccinesReferralsPaediatricsRare diseasesRegulatory and procedural guidanceClinical trialsAdvanced therapiesData on medicinesCompliance and inspectionsInnovationResearch and developmentMedicine shortagesBiosimilarsSMEAntimicrobial resistanceGovernanceBrexitQuality of medicinesCorporateGeneric and hybrid medicinesEarly accessMedicines for use outside the EUFeesProduct informationScientific adviceMedical devicesMaximum residue limitMpoxBiologicalsScientific guidelinesVeterinary limited marketsCompassionate useCareersMedication errorParallel distributionPRIMEProcurement Diseases area Viral diseasesCancerImmune-system diseasesDiabetesNeurodegenerative diseasesCardiovascular diseasesHIV and AIDS Responsible body CHMP CVMP PRAC Management Board COMP PDCO CMDh HMPC CAT Patient safety Yes Efterlad dette felt tomt Filter Resultater (3800) Sort by Last update date (new to old)Last update date (old to new)A-ZZ-A Efterlad dette felt tomt Concept paper on fees for new pharmacovigilance activities released for public consultation 20 juni 2012NewsCorporate Committee for Orphan Medicinal Products (COMP) June 2012 highlights 18 juni 2012NewsHumanRare diseases European Medicines Agency website on suspected side effect reports now in all 23 EU official languages 18 juni 2012NewsCorporateMedicines Committee for Medicinal Products for Veterinary Use (CVMP) meeting of 12-14 June 2012 15 juni 2012Press releaseVeterinary European Medicines Agency finalises guidance on medicines containing monoclonal antibodies 15 juni 2012NewsHumanMedicines Management Board completes framework for conflicts of interests 8 juni 2012Press releaseCorporate European Medicines Agency welcomes 1000th orphan designation 7 juni 2012NewsCorporateMedicines European Medicines Agency launches new electronic form for submission of plasma-master-file applications 7 juni 2012NewsCorporateMedicines Annual report 2011 shows continuously high level of activities 6 juni 2012NewsCorporate Revised guideline on quality of biosimilar medicines open for comments 31 maj 2012NewsHumanBiosimilarsRegulatory and procedural guidance 1 … 247 248 249 250 251 Page 251 of 380 252 253 254 255 … 380
Concept paper on fees for new pharmacovigilance activities released for public consultation 20 juni 2012NewsCorporate
Committee for Orphan Medicinal Products (COMP) June 2012 highlights 18 juni 2012NewsHumanRare diseases
European Medicines Agency website on suspected side effect reports now in all 23 EU official languages 18 juni 2012NewsCorporateMedicines
Committee for Medicinal Products for Veterinary Use (CVMP) meeting of 12-14 June 2012 15 juni 2012Press releaseVeterinary
European Medicines Agency finalises guidance on medicines containing monoclonal antibodies 15 juni 2012NewsHumanMedicines
European Medicines Agency launches new electronic form for submission of plasma-master-file applications 7 juni 2012NewsCorporateMedicines
Revised guideline on quality of biosimilar medicines open for comments 31 maj 2012NewsHumanBiosimilarsRegulatory and procedural guidance