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Shaping EU medicines regulation in the post COVID-19 era.
Cavaleri, Marco; Sweeney, Fergus; Gonzalez-Quevedo, Rosa; Carr, Melanie.
Afiliação
  • Cavaleri M; European Medicines Agency, Chair COVID-19 Task Force, Domenico Scarlattilaan 6, 1083 HS Amsterdam, The Netherlands.
  • Sweeney F; European Medicines Agency, Head of Clinical Studies and Manufacturing Task Force, Domenico Scarlattilaan 6, 1083 HS Amsterdam, The Netherlands.
  • Gonzalez-Quevedo R; European Medicines Agency, Stakeholders and Communication Division, Domenico Scarlattilaan 6, 1083 HS Amsterdam, The Netherlands.
  • Carr M; European Medicines Agency, Head of Stakeholders and Communication Division, Domenico Scarlattilaan 6, 1083 HS Amsterdam, The Netherlands.
Lancet Reg Health Eur ; 9: 100192, 2021 Oct.
Article em En | MEDLINE | ID: mdl-34661185
The EU Medicines Regulatory Network (EMRN), comprised of the European Medicines Agency (EMA), the medicines regulatory authorities of the Member States and the European Commission (EC), is operating amid a complex crisis that has positioned regulators centre stage due to their key role in the development, approval and safety monitoring of vaccines and treatments for COVID-19. Here we consider the EMA's and EMRN's response to the pandemic and some of the early learnings that will help reshape medicines regulation in the post COVID-19 era. We also reflect on how some of these learnings will be formally followed up under revised EU legislation to extend EMA's mandate, reinforcing its role in crisis preparedness and response.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: Lancet Reg Health Eur Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Holanda

Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: Lancet Reg Health Eur Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Holanda