Clinical Research Training Program
Train healthcare professionals and future clinical researchers in international clinical research methodologies, tools, legislation, and good clinical practices (ICH-GCP). This program focuses on the regulatory, ethical, and procedural requirements in Portugal, Europe, and globally, providing the skills for autonomous biomedical and clinical research in both academic and business environments.
The aim of this product is to train the human resources of clinical research centers (doctors, nurses, pharmacists, study coordinators) and other professionals who have a potential interest in developing clinical studies in the future, in new methodologies, tools, legislation, and good clinical practices (ICH-GCP), determined internationally for the harmonization/uniformity of procedures in clinical research.
The training component should guarantee knowledge of the regulatory, ethical, procedural, and technical requirements in force in Portugal, Europe, and the rest of the world. The program's main objective is to train researchers with biomedical and clinical research skills in an autonomous way, both in an academic environment and in a business environment, and in healthcare institutions.