The European Medicines Agency (EMA) publishes open letters, usually in response to contributions and feedback from stakeholders.

Replies to open letters from Members of the European Parliament concerning the marketing authorisations of mRNA COVID-19 vaccines

Reply in follow up to the COVI exchange of views on 27 March 2023

Reply to open letter from Members of the European Parliament's letter on psychedelic-assisted therapies

Reply to open letter from Members of the European Parliament concerning COVID-19 vaccines

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Reply to open letter from ‘Doctors for COVID ethics’ concerning COVID-19 vaccines

Reply to open letter concerning COVID-19 vaccines

Letter from the chairs of EMA's Management Board to Guido Rasi at the end of his term as EMA's Executive Director

Reply to open letter concerning the transparency and evaluation of vaccines for COVID-19

Response to the European Ombudsman concerning transparency and independence of EMA's work in supporting the development and evaluation of COVID-19 medicines

Response to European Ombudsman regarding pre-submission activities

Response to Nordic Cochrane Centre on safety review of human papillomavirus vaccines

Clarifying the adaptive pathways concept

Response to European Ombudsman explaining redaction rules

Response to European Ombudsman on clinical trial data transparency

Letter to Member of European Parliament requesting correction

Response to British Medical Journal editorial on the new Agency

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