Events

Committee for Medicinal Products for Human Use (CHMP): 22-25 January 2024

The Committee for Medicinal Products for Human Use (CHMP) is the committee that is responsible for preparing the Agency's opinions on all questions concerning human medicines.

European Medicines Agency, Amsterdam, the Netherlands
Data iniziale: 22 Gennaio 2024
Data finale: 25 Gennaio 2024
Event Human Medicines
Committee for Advanced Therapies (CAT): 17-19 January 2024

The Committee for Advanced Therapies (CAT) is the committee that is responsible for assessing the quality, safety and efficacy of advanced-therapy medicines.

European Medicines Agency, Amsterdam, the Netherlands
Data iniziale: 17 Gennaio 2024
Data finale: 19 Gennaio 2024
Event Human Advanced therapies Innovation
Committee for Orphan Medicinal Products (COMP): 16-18 January 2024

The Committee for Orphan Medicinal Products (COMP) is the committee that is responsible for reviewing applications for 'orphan medicinal product designation' for medicines intended for the diagnosis, prevention or treatment of rare diseases.

European Medicines Agency, Amsterdam, the Netherlands
Data iniziale: 16 Gennaio 2024
Data finale: 18 Gennaio 2024
Event Human Rare diseases
Paediatric Committee (PDCO): 16-19 January 2024

The Paediatric Committee (PDCO) is the committee that is responsible for assessing the content of paediatric investigation plans, which describe how a medicine should be studied in children, as well as waivers and deferrals.

European Medicines Agency, Amsterdam, the Netherlands
Data iniziale: 16 Gennaio 2024
Data finale: 19 Gennaio 2024
Event Human Paediatrics
Committee for Medicinal Products for Veterinary Use (CVMP): 16-18 January 2024

The Committee for Medicinal Products for Veterinary Use (CVMP) is the committee that is responsible for preparing the Agency's opinions on all questions concerning veterinary medicines.

European Medicines Agency, Amsterdam, the Netherlands
Data iniziale: 16 Gennaio 2024
Data finale: 18 Gennaio 2024
Event Veterinary Medicines
Webinar on the Union Product Database Data Quality Framework

National competent authorities are invited to attend this session for a progress report on UPD Data Quality Framework

Online
European Medicines Agency, Amsterdam, the Netherlands
Data iniziale: 11 Gennaio 2024, 15:00 (CET)
Data finale: 11 Gennaio 2024, 16:30 (CET)
Event Veterinary Medicines
Pharmacovigilance Risk Assessment Committee (PRAC): 8-11 January 2024

The Pharmacovigilance Risk Assessment Committee (PRAC) is the committee that is responsible for assessing all aspects of the risk management of medicines for human use.

European Medicines Agency, Amsterdam, the Netherlands
Data iniziale: 8 Gennaio 2024
Data finale: 11 Gennaio 2024
Event Human Pharmacovigilance
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