Guidance notes on the use of Veterinary Dictionary for Drug Regulatory Activities (VeDDRA) terminology for reporting suspected adverse events in animals and humans - Rev.16

Submitted by Anonymous (not verified) on 26 July 2024 - 9:33

Guidance notes on the use of Veterinary Dictionary for Drug Regulatory Activities (VeDDRA) terminology for reporting suspected adverse events in animals and humans - Rev.16

Combined Veterinary Dictionary for Drug Regulatory Activities (VeDDRA) list of clinical terms for reporting suspected adverse events in animals and humans to veterinary medicinal products - Rev.15

Submitted by Anonymous (not verified) on 26 July 2024 - 9:27

Combined Veterinary Dictionary for Drug Regulatory Activities (VeDDRA) list of clinical terms for reporting suspected adverse events in animals and humans to veterinary medicinal products - Rev.15

Committee for Medicinal Products for Veterinary Use (CVMP): 18-20 June 2024, European Medicines Agency, Amsterdam, the Netherlands, from 18 June 2024 to 20 June 2024

Submitted by Anonymous (not verified) on 25 July 2024 - 14:15

Committee for Medicinal Products for Veterinary Use (CVMP): 18-20 June 2024, European Medicines Agency, Amsterdam, the Netherlands, from 18 June 2024 to 20 June 2024

European Medicines Agency (EMA) Patients' and Consumers' (PCWP) and Healthcare Professionals' (HCPWP) Working Parties joint meeting, European Medicines Agency, Amsterdam, the Netherlands, from 2 July 2024 to 3 July 2024

Submitted by Anonymous (not verified) on 25 July 2024 - 14:06

European Medicines Agency (EMA) Patients' and Consumers' (PCWP) and Healthcare Professionals' (HCPWP) Working Parties joint meeting, European Medicines Agency, Amsterdam, the Netherlands, from 2 July 2024 to 3 July 2024

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