The European medicines regulatory system is based on a network of around 50 regulatory authorities from the. 31 EEA countries (28 EU Member States plus Iceland.
5 mai 2017 REGULATION (EU) 2017/745 OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL of 5 April 2017 on medical devices amending Directive 2001/83/EC
4 mai 2016 REGULATION (EU) 2016/679 OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL of 27 April 2016 on the protection of natural persons with regard to ...
8 août 2017 Consequently an EU Regulatory Network Incident Management Plan for medicines for human use was developed. A pilot phase was started in ...
13 mars 2018 supplementing Directive (EU) 2015/2366 of the European Parliament and of the Council with regard to regulatory technical standards for ...
4 oct. 2021 interest as part of their ongoing financial regulatory dialogue. EU participants included representatives of the European Commission the ...
9 déc. 2019 REGULATION (EU) 2019/2088 OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL of 27 November 2019 on sustainability?related disclosures in the ...
The ESAs also set out options to be considered in the context of future EU-level work on innovation facilitators
17 mars 2022 In December 2020 the European Commission tabled a proposal to modernise the regulatory framework for batteries and secure the sustainability ...
18 juin 2020 Regulation (EU) 2019/2088 only considers an investment to be a sustainable investment if it does not significantly.