After finishing the second module on 24 June and taking a holiday period, the “Expert on Regulatory Affairs” course starts on 9 September. Every Friday, until 2 December, the second block of the course will take place with modules 3 (Design, development and production), 4 (Usability Evaluation), 5 (Clinical evaluation) and 6 (Clinical trial management).
The lecturers for modules 3, 4, 5 and 6 are the following:
- Miguel Angel Campanero (A3Z Advanced)
- Begoña Alonso Gómez (BEALIA Servicios Técnicos y de Consultoría, S.L.)
- Rocío Díaz (Quirón)
- Isabel Gil (Navarrabiomed, Centro de Investigación Biomédica)
- Jon Mabe (Tekniker)
- Digna González(Bexen Cardio)
- Silvia Almaraz (Bexen Cardio)
- María Paños Correas (Allergan)
- Concepción Rodríguez (Agencia Española de Medicamentos y Productos Sanitarios)
- Ana Mª Villarta Aguilera (Agencia Española de Medicamentos y Productos Sanitarios)
- Gloria Hernández (Agencia Española de Medicamentos y Productos Sanitarios)
- Silvia Martín (Agencia Española de Medicamentos y Productos Sanitarios)
Module 5 is full. But there are still some places left for the other modules. As on previous occasions, registration will close on the Friday before the start of the module. That’s why you have until the following dates to register:
- M3: 2 September
- M4: 7th October
- M6: 18 November
- M7: 6 January 2023
- M8: 20 January 2023
- M final: 3 February 2023
The course follows the combined methodology of theory and practice through lectures and group workshops. Classes will be held on Fridays, from 09:30 to 13:30, at BIC Bizkaia: Camino Astondo, Edificio 612, 48160 Derio, Parque Científico y Tecnológico de Vizcaya.
For more information and to download the program (in Spanish) click on the following button:
