As Brexit is quickly coming closer, the CMDh has published an updated version of the Practical guidance for procedures related to Brexit for medicinal products for human use approved via MRP/DCP in...
The United Kingdom (UK) has left the European Union (EU) and the transition period after Brexit comes to an end this year and from 1 January 2021 new regulations will apply. These changes will also af...
From 1 January 2021, the Medicines and Healthcare products Regulatory Agency (MHRA) will be the UK’s standalone medicines and medical devices regulator.
La Agencia Reguladora de Medicamentos y Productos Sanitarios del Reino Unido (MHRA) ha publicado una nota informativa de los requisitos para comercializar productos sanitarios en UK desde 1 de Enero d...
Según José María Ferrer, responsable del departamento de Legislación de AINIA Centro Tecnológico, las áreas afectadas en las relaciones entre Reino Unido y la Unión Europea serán el etiquetado...