Products Management Services (PMS) - Implementation of International Organization for Standardization (ISO) standards for the identification of medicinal products (IDMP) in Europe - Chapter 1: Registration requirements

Submitted by Anonymous (not verified) on 12 December 2024 - 12:00

Products Management Services (PMS) - Implementation of International Organization for Standardization (ISO) standards for the identification of medicinal products (IDMP) in Europe - Chapter 1: Registration requirements

Meeting of the Executive Steering Group on Shortages and Safety of Medicinal Products (MSSG) - November 2024, Online, European Medicines Agency, Amsterdam, the Netherlands, from 19 November 2024, 12:30 (CET) to 19 November 2024, 14:30 (CET)

Submitted by Anonymous (not verified) on 12 December 2024 - 12:00

Meeting of the Executive Steering Group on Shortages and Safety of Medicinal Products (MSSG) - November 2024, Online, European Medicines Agency, Amsterdam, the Netherlands, from 19 November 2024, 12:30 (CET) to 19 November 2024, 14:30 (CET)

Human medicines European public assessment report (EPAR): Cystadane, betaine anhydrous, Date of authorisation: 14/02/2007, Revision: 15, Status: Authorised

Submitted by Anonymous (not verified) on 12 December 2024 - 10:11

Human medicines European public assessment report (EPAR): Cystadane, betaine anhydrous, Date of authorisation: 14/02/2007, Revision: 15, Status: Authorised

Human medicines European public assessment report (EPAR): Isturisa, osilodrostat, Date of authorisation: 09/01/2020, Revision: 7, Status: Authorised

Submitted by Anonymous (not verified) on 12 December 2024 - 9:53

Human medicines European public assessment report (EPAR): Isturisa, osilodrostat, Date of authorisation: 09/01/2020, Revision: 7, Status: Authorised

Clinical Trial Information System (CTIS) structured data form - Initial application, additional Member State Concerned, substantial modification, non-substantial modification

Submitted by Anonymous (not verified) on 11 December 2024 - 15:55

Clinical Trial Information System (CTIS) structured data form - Initial application, additional Member State Concerned, substantial modification, non-substantial modification

Template for submission of comments for the Veterinary Dictionary for Drug Regulatory Activities (VeDDRA) standard list for EudraVigilance Veterinary (EVVet)

Submitted by Anonymous (not verified) on 11 December 2024 - 15:05

Template for submission of comments for the Veterinary Dictionary for Drug Regulatory Activities (VeDDRA) standard list for EudraVigilance Veterinary (EVVet)

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