Procurement

Additional information - Applicant’s clarifications following Paediatric Committee (PDCO) discussions or re-discussions

Response to Paediatric Committee request for supplementary information and modification of proposed PIP (RSI) - Re-submission following clock-stop

Key elements form: Applicant’s proposal for a paediatric-investigation-plan opinion

Template for scientific document for paediatric investigation plan or product-specific waiver

Procedural advice on paediatric applications

Human medicines European public assessment report (EPAR): Voriconazole Accord, voriconazole, Date of authorisation: 16/05/2013, Revision: 21, Status: Authorised

COVID-19 vaccines: key facts

EMA workshop on primary efficacy endpoints for antivirals and monoclonal antibodies intended for the treatment of COVID-19 and influenza, Online, European Medicines Agency, Amsterdam, the Netherlands, Broadcast, from 5 June 2025, 13:00 (CEST) to 6 June 2025, 17:00 (CEST)

Substances considered as not falling within the scope of Regulation (EC) No. 470/2009, with regard to residues of veterinary medicinal products in foodstuffs of animal origin