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Last updated about 22 hours ago
Minimum inhibitory concentration (MIC) breakpoints
about 22 hours ago
Minimum inhibitory concentration (MIC) breakpoints
Human medicines European public assessment report (EPAR): Trepulmix, treprostinil, Date of authorisation: 03/04/2020, Revision: 5, Status: Authorised
about 23 hours ago
Human medicines European public assessment report (EPAR): Trepulmix, treprostinil, Date of authorisation...
Human medicines European public assessment report (EPAR): Ajovy, fremanezumab, Date of authorisation: 28/03/2019, Revision: 11, Status: Authorised
about 23 hours ago
Human medicines European public assessment report (EPAR): Ajovy, fremanezumab, Date of authorisation...
Human medicines European public assessment report (EPAR): Voydeya, Danicopan, Date of authorisation: 19/04/2024, Status: Authorised
about 23 hours ago
Human medicines European public assessment report (EPAR): Voydeya, Danicopan, Date of authorisation...
Clinical Trials Information System (CTIS) Bitesize Talk: Revised transparency rules and the new CTIS public portal, European Medicines Agency, Amsterdam, the Netherlands, Broadcast, from 20 June 2024, 15:30 (CEST) to 20 June 2024, 17:00 (CEST)
about 23 hours ago
Clinical Trials Information System (CTIS) Bitesize Talk: Revised transparency rules and the...
On-boarding of users to Substance, Product, Organisation and Referentials (SPOR) data services
about 23 hours ago
On-boarding of users to Substance, Product, Organisation and Referentials (SPOR) data services
Human medicines European public assessment report (EPAR): Onivyde pegylated liposomal (previously known as Onivyde), irinotecan hydrochloride trihydrate, Date of authorisation: 14/10/2016, Revision: 12, Status: Authorised
about 23 hours ago
Human medicines European public assessment report (EPAR): Onivyde pegylated liposomal (previously known...
Outcomes of imposed non-interventional post-authorisation safety studies
about 24 hours ago
Outcomes of imposed non-interventional post-authorisation safety studies
European Medicines Agency’s data protection notice for the EMA Help Desk
about 24 hours ago
European Medicines Agency’s data protection notice for the EMA Help Desk
Products Management Services (PMS) - Implementation of International Organization for Standardization (ISO) standards for the identification of medicinal products (IDMP) in Europe - Chapter 1
about 24 hours ago
Products Management Services (PMS) - Implementation of International Organization for Standardization (ISO)...
Human medicines European public assessment report (EPAR): Miglustat Gen.Orph, miglustat, Date of authorisation: 09/11/2017, Revision: 10, Status: Authorised
1 day ago
Human medicines European public assessment report (EPAR): Miglustat Gen.Orph, miglustat, Date of...
Hydroxyprogesterone caproate medicines to be suspended from the EU market
1 day ago
Hydroxyprogesterone caproate medicines to be suspended from the EU market