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 How big data can be used for the development and regulation of medicines 8 November 2016NewsCorporate Workshop: working towards new therapies for spinal muscular atrophy 7 November 2016NewsCorporate Webinar on regulatory and procedural aspects of applications for type I variations 4 November 2016NewsCorporate Meeting highlights from the Pharmacovigilance Risk Assessment Committee (PRAC) 24-27 October 2016 28 October 2016NewsHumanPharmacovigilance EMA closed from 28 October to 3 November 2016 27 October 2016NewsCorporate New search page for periodic safety update report single assessments (PSUSAs) 26 October 2016NewsCorporate Regulatory update – EMA encourages companies to submit Type I variations for 2016 by end of November 24 October 2016NewsCorporate How to make better use of patient registries to collect high-quality data on medicines 24 October 2016NewsCorporate Opening up clinical data on new medicines 20 October 2016Press releaseCorporate Regulatory information – Updated SME user guide now available 19 October 2016NewsCorporateSME 1 … 146 147 148 149 150 Page 150 of 380 151 152 153 154 … 380
How big data can be used for the development and regulation of medicines 8 November 2016NewsCorporate
Webinar on regulatory and procedural aspects of applications for type I variations 4 November 2016NewsCorporate
Meeting highlights from the Pharmacovigilance Risk Assessment Committee (PRAC) 24-27 October 2016 28 October 2016NewsHumanPharmacovigilance
New search page for periodic safety update report single assessments (PSUSAs) 26 October 2016NewsCorporate
Regulatory update – EMA encourages companies to submit Type I variations for 2016 by end of November 24 October 2016NewsCorporate
How to make better use of patient registries to collect high-quality data on medicines 24 October 2016NewsCorporate
