Филтриране по Last updated date SelectСледПредиFrom - To Дата Крайна дата This week This month Last week Last month 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 Leave this field blank Filter Резултати (3799) Sort by Last update date (new to old)Last update date (old to new)A-ZZ-A Leave this field blank Update on review of valsartan medicines: risk from NDMA remains low, a related substance NDEA also being investigated 13 September 2018Press releaseHumanMedicinesReferrals Meeting highlights from the Pharmacovigilance Risk Assessment Committee (PRAC) 3-6 September 2018 7 September 2018NewsHumanPharmacovigilance Development of medicines for rare diseases 31 August 2018NewsCorporate Towards improving the availability of medicines in the EU 29 August 2018Press releaseCorporate Fostering medicines for children 28 August 2018NewsCorporatePaediatrics European Medicines Agency closed 27 August 2018 23 August 2018NewsCorporateMedicines Keeping medicines safe 22 August 2018NewsCorporate Update on medicines containing valsartan from Zhejiang Tianyu: company no longer authorised to manufacture valsartan active substance for EU medicines due to presence of NDMA 20 August 2018Press releaseCorporate How are new medicines approved by EMA? 15 August 2018NewsCorporate Update on review of valsartan medicines due to detection of NDMA: EMA reviewing valsartan produced by another company Zhejiang Tianyu 10 August 2018Press releaseHumanMedicines 1 … 112 113 114 115 116 Page 116 of 380 117 118 119 120 … 380
Update on review of valsartan medicines: risk from NDMA remains low, a related substance NDEA also being investigated 13 September 2018Press releaseHumanMedicinesReferrals
Meeting highlights from the Pharmacovigilance Risk Assessment Committee (PRAC) 3-6 September 2018 7 September 2018NewsHumanPharmacovigilance
Update on medicines containing valsartan from Zhejiang Tianyu: company no longer authorised to manufacture valsartan active substance for EU medicines due to presence of NDMA 20 August 2018Press releaseCorporate
Update on review of valsartan medicines due to detection of NDMA: EMA reviewing valsartan produced by another company Zhejiang Tianyu 10 August 2018Press releaseHumanMedicines