The Council has adopted new rules aimed at improving the safety and quality of blood, tissues and cells used in healthcare and facilitating cross-border circulation of these substances in the EU. Read the press release published by the...
Presented to Parliament pursuant to section 46(1) of the Medicines and Medical Devices Act 2021. The Medicines and Medical Devices Act (MMDA) became law in February 2021. The act provides the Secretary of State for Health and...
Report on all regulations in force during the first reporting period made using the powers in specific sections of the act, including stakeholder feedback and the department’s response. This report provides an overview of all...
The aim of this consultation is to seek the views of stakeholders on proposals to amend the Human Medicines Regulations 2012 (HMRs) to remove remaining references to organisations in England and Northern Ireland which have since been...
The Council review of disagreements that arise in the care of critically ill children in England recommends the creation of a Government taskforce to take forward the changes our evidence has shown will help reduce...
The video recording and presentation materials of the webinar Awareness session for SMEs on the reform of the EU pharmaceutical legislation held the 24 November 2023 is now available on the EMA website. Event summary...
“Un accord sur le règlement sur les substances d’origine humaine (SoHO) a été trouvé ce jeudi 14 décembre à Bruxelles entre le Parlement européen, le Conseil de l’UE et la Commission européenne.” https://www.efs.sante.fr/reglement-europeen-soho-un-accord-trouve-bruxelles
“Jeudi 18 janvier 2024, l’Office a entendu Marine Jeantet, directrice générale de l’Agence de la biomédecine, sur les évolutions récentes des connaissances et des techniques dans les domaines relevant des lois de bioéthique.” https://www.assemblee-nationale.fr/dyn/16/organes/delegations-comites-offices/opecst/actualites/evolutions-recentes-dans-les-domaines-relevant-des-lois-de-bioethique-audition-de-l-agence-de-la-biomedecine
In the report, data are discussed on cross-border patient healthcare following Directive 2011/24/EU for reference year 2021. Read the news announcement published by EC Directorate-General for Health and Food Safety on 6 June 2023.
