AECIC (Asociación Española de Compañías de Investigación Clínica/Spanish association of CROs) is aware of the continuous development and innovation in clinical research. Thus, it is necessary to include improvements and changes in daily processes in order to enhance working results and follow the evolution of clinical research.
For this reason, on November 12th 2019, AECIC is offering a conference session about EU 536/2014 Regulation for clinical trials of medicinal products for human, next steps for 2020. In this session, it will be discussed the state of the art from several points of view as Spanish and European Health Authorities, Pharmaceutical Companies, CROs and Health Institutions.
For more information: VIII Jornadas AECIC – Aplicación del Reglamento UE 536/2014 de ensayos clínicos.
