Policy 78: EMA environmental policy
Submitted by Anonymous (not verified) on 15 May 2024 - 15:19
Policy 78: EMA environmental policy
Agenda of the PRAC meeting 13-16 May 2024
Submitted by Anonymous (not verified) on 14 May 2024 - 17:00
Agenda of the PRAC meeting 13-16 May 2024
Pharmacovigilance Risk Assessment Committee (PRAC): 13-16 May 2024, European Medicines Agency, Amsterdam, the Netherlands, from 13 May 2024 to 16 May 2024
Submitted by Anonymous (not verified) on 14 May 2024 - 17:00
Pharmacovigilance Risk Assessment Committee (PRAC): 13-16 May 2024, European Medicines Agency, Amsterdam, the Netherlands, from 13 May 2024 to 16 May 2024
Guidebook for tenderers
Submitted by Anonymous (not verified) on 14 May 2024 - 16:15
Guidebook for tenderers
Article 57 product data
Submitted by Anonymous (not verified) on 14 May 2024 - 15:38
Article 57 product data
Human medicines European public assessment report (EPAR): Olanzapine Mylan, olanzapine, Date of authorisation: 06/10/2008, Revision: 20, Status: Authorised
Submitted by Anonymous (not verified) on 14 May 2024 - 13:37
Human medicines European public assessment report (EPAR): Olanzapine Mylan, olanzapine, Date of authorisation: 06/10/2008, Revision: 20, Status: Authorised
Minutes of the PRAC meeting 4-7 March 2024
Submitted by Anonymous (not verified) on 14 May 2024 - 13:24
Minutes of the PRAC meeting 4-7 March 2024
Products Management Services (PMS) - Implementation of International Organization for Standardization (ISO) standards for the identification of medicinal products (IDMP) in Europe - Chapter 1
Submitted by Anonymous (not verified) on 14 May 2024 - 11:11
Products Management Services (PMS) - Implementation of International Organization for Standardization (ISO) standards for the identification of medicinal products (IDMP) in Europe - Chapter 1
On-boarding of users to Substance, Product, Organisation and Referentials (SPOR) data services
Submitted by Anonymous (not verified) on 14 May 2024 - 10:00
On-boarding of users to Substance, Product, Organisation and Referentials (SPOR) data services
Products Management Services - Implementation of International Organization for Standardization (ISO) standards for the identification of medicinal products (IDMP) in Europe: Introduction - EU Implementation Guide
Submitted by Anonymous (not verified) on 14 May 2024 - 8:48
Products Management Services - Implementation of International Organization for Standardization (ISO) standards for the identification of medicinal products (IDMP) in Europe: Introduction - EU Implementation Guide