Do you want to know more about ISO IDMP implementation? Our Director of Regulatory Information, Remco Munnik, and Ana Orozco from AEFI will be running a course about it: “Jornada sobre la implementación del IDMP (Identification of Medicinal Products) y manejo de Datos” on 5th July in Madrid. To register and for more information click here: http://bit.ly/29aBvfU
Brexit updates for human use medicinal products approved via MRP/DCP
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 December 2020.