Φιλτράρισμα ανά Last updated date SelectΜετάΠρινFrom - To Date Ημερομηνία λήξης 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 Αποτελέσματα (3839) Sort by Last update date (new to old)Last update date (old to new)A-ZZ-A Leave this field blank Meeting highlights from the Committee for Medicinal Products for Human Use,20-23 October 2008 24 Οκτώβριος 2008Press releaseHuman Meeting highlights from the Paediatric Committee: 15 - 17 October 2008 24 Οκτώβριος 2008Press releaseHumanPaediatrics The European Medicines Agency recommends suspension of the marketing authorisation of Acomplia 23 Οκτώβριος 2008Press releaseHumanMedicines European Medicines Agency recommends first switch from prescription-only to non-prescription for a centrally authorised medicine 23 Οκτώβριος 2008Press releaseHumanMedicines Committee for medicinal products for veterinary use: Meeting of 14-16 October 2008 17 Οκτώβριος 2008Press releaseVeterinary Wyeth Europa Ltd withdraws its marketing authorisation application for Ellefore 15 Οκτώβριος 2008Press release EMEA half-year report for 2008 shows activities to be on target, with a marked increase in the provision of scientific advice 8 Οκτώβριος 2008Press releaseCorporate Medicines regulators on both sides of the Atlantic confirm commitment to cooperation on medicines 7 Οκτώβριος 2008Press releaseMedicines Public statement on the current shortage of radiopharmaceuticals in the European Union 1 Οκτώβριος 2008News Meeting highlights from the Paediatric Committee: 17 - 19 September 2008 28 Σεπτέμβριος 2008Press releaseHumanPaediatrics 1 … 309 310 311 312 313 Page 313 of 384 314 315 316 317 … 384
Meeting highlights from the Committee for Medicinal Products for Human Use,20-23 October 2008 24 Οκτώβριος 2008Press releaseHuman
Meeting highlights from the Paediatric Committee: 15 - 17 October 2008 24 Οκτώβριος 2008Press releaseHumanPaediatrics
The European Medicines Agency recommends suspension of the marketing authorisation of Acomplia 23 Οκτώβριος 2008Press releaseHumanMedicines
European Medicines Agency recommends first switch from prescription-only to non-prescription for a centrally authorised medicine 23 Οκτώβριος 2008Press releaseHumanMedicines
Committee for medicinal products for veterinary use: Meeting of 14-16 October 2008 17 Οκτώβριος 2008Press releaseVeterinary
Wyeth Europa Ltd withdraws its marketing authorisation application for Ellefore 15 Οκτώβριος 2008Press release
EMEA half-year report for 2008 shows activities to be on target, with a marked increase in the provision of scientific advice 8 Οκτώβριος 2008Press releaseCorporate
Medicines regulators on both sides of the Atlantic confirm commitment to cooperation on medicines 7 Οκτώβριος 2008Press releaseMedicines
Public statement on the current shortage of radiopharmaceuticals in the European Union 1 Οκτώβριος 2008News
Meeting highlights from the Paediatric Committee: 17 - 19 September 2008 28 Σεπτέμβριος 2008Press releaseHumanPaediatrics