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 Regulatory information - Adjusted fees for applications to European Medicines Agency from 1 April 2015 26 februar 2015NewsCorporateMedicines Rare Disease Day 2015 26 februar 2015NewsCorporate Regulatory information - Transitioning to mandatory use of electronic application forms 25 februar 2015NewsCorporate Regulatory information - EMA introduces weekly start dates for the assessment of type II variations from March 2015 20 februar 2015NewsCorporate Regulatory information - Committee chairs' handwritten signatures no longer included in opinion documents from March 2015 20 februar 2015NewsCorporate Identification of medicines: EU task force to implement new international standards 20 februar 2015NewsCorporate Safety signals: recommendations now available in all EU languages 18 februar 2015NewsHumanPharmacovigilance Major European research project on monitoring and evaluation of medicines concludes 16 februar 2015NewsCorporate Committee for Medicinal Products for Veterinary Use (CVMP) Meeting of 10-12 February 2015 13 februar 2015Press releaseVeterinary Meeting highlights from the Pharmacovigilance Risk Assessment Committee (PRAC) 9-12 February 2015 13 februar 2015NewsHumanPharmacovigilance 1 … 179 180 181 182 183 Page 183 of 380 184 185 186 187 … 380
Regulatory information - Adjusted fees for applications to European Medicines Agency from 1 April 2015 26 februar 2015NewsCorporateMedicines
Regulatory information - Transitioning to mandatory use of electronic application forms 25 februar 2015NewsCorporate
Regulatory information - EMA introduces weekly start dates for the assessment of type II variations from March 2015 20 februar 2015NewsCorporate
Regulatory information - Committee chairs' handwritten signatures no longer included in opinion documents from March 2015 20 februar 2015NewsCorporate
Identification of medicines: EU task force to implement new international standards 20 februar 2015NewsCorporate
Safety signals: recommendations now available in all EU languages 18 februar 2015NewsHumanPharmacovigilance
Major European research project on monitoring and evaluation of medicines concludes 16 februar 2015NewsCorporate
Committee for Medicinal Products for Veterinary Use (CVMP) Meeting of 10-12 February 2015 13 februar 2015Press releaseVeterinary
Meeting highlights from the Pharmacovigilance Risk Assessment Committee (PRAC) 9-12 February 2015 13 februar 2015NewsHumanPharmacovigilance