Author:
Capello Daniela,Rimedio Antonio
Publisher
Springer International Publishing
Reference11 articles.
1. Calvert M, Kyte D, Mercieca-Bebber R, Slade A, Chan A-W, King MT, SPIRIT-PRO Group, Hunn A, Bottomley A, Regnault A, Ells C, O’Connor D, Revicki D, Patrick D, Altman D, Bash E, Velikova G, Price G, Draper H, Blazeby J, Scott J, Groves T (2018) Guidelines for inclusion of patient-reported outcomes in clinical trial protocols: the SPIRIT-PRO extension. JAMA 6:483–494. https://doi.org/10.1001/jama.2017.21903
2. Cippitani R (2019) Ethics advisor on research projects. In: Bartolini A, Cippitani R, Colcelli V (eds) Dictionary of statuses within EU law (the individual statuses as pillar of European Union integration). Springer Nature, Cham, pp 193–200
3. Hallinan D (2020) Broad consent under the GDPR: an optimistic perspective on a bright future. Life Sci Soc Policy 16:1. https://doi.org/10.1186/s40504-019-0096-3
4. Hamerlijnck D (2017) The importance of patient involvement in clinical trials. ERS – Respiratory Equipment and Devices Exhibition Magazine. https://3qksc436bu713cqimwcfglyj-wpengine.netdna-ssl.com
5. Jacobs G, Wolf A, Krawczak M, Lieb W (2018) Biobanks in the era of digital medicine. Clin Pharmacol Ther 103(5):761–762. https://doi.org/10.1002/cpt.968