An EU Comparative Analysis of the Regulation of Clinical Trials Supervisory Bodies in the Aftermath of Regulation 536/2014

Autor: Miguel Beriain, Iñigo, Chortara, Theodora, Duardo-Sánchez, Aliuska, Feeney, Oliver, Felzmann, Heike, Fernández, Emma U., Lievevrouw, Elisa, Marelli, Luca, Mattsson, Titti, Rothmar Herrmann, Janne, Minssen, Timo, Pulice, Elisabetta, Vera Lúcia Carapeto Raposo, Robienski, Jürgen, Penasa, Simone, Hoyweghen, Ine

Publikováno v: Lund University
Addi: Archivo Digital para la Docencia y la Investigación
Universidad del País Vasco
Universidade Nova de Lisboa
Scopus-Elsevier
Addi. Archivo Digital para la Docencia y la Investigación
instname
University of Copenhagen
Universidad de Cantabria (UC)
CIÊNCIAVITAE

The new EU regulation on clinical trials is intended to promote a greater level of harmonization of European Union rules in this area. However, it does not elaborate a common normative framework regarding the functioning of research ethics committees

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::91d989d360e737e67b142e6e6bd4a471
https://portal.research.lu.se/en/publications/59844192-5149-41fa-9f3c-3c1043a17bd8