No edit summary |
No edit summary |
||
Line 2: | Line 2: | ||
|Number = 161 | |Number = 161 | ||
|Title = Consenting to the Participation in Clinical Trials | |Title = Consenting to the Participation in Clinical Trials | ||
|Content = For the purpose of consenting to the participation in scientific research activities in clinical trials, the relevant provisions of Regulation (EU) No 536/2014 of the European Parliament and of the Council<ref>Regulation (EU) No 536/2014 of the European Parliament and of the Council of 16 April 2014 on clinical trials on medicinal products for human use, and repealing Directive 2001/20/EC | |Content = For the purpose of consenting to the participation in scientific research activities in clinical trials, the relevant provisions of Regulation (EU) No 536/2014 of the European Parliament and of the Council<ref>Regulation (EU) No 536/2014 of the European Parliament and of the Council of 16 April 2014 on clinical trials on medicinal products for human use, and repealing Directive 2001/20/EC should apply. | ||
}} | }} |
Latest revision as of 10:14, 6 September 2021
Recital 161: Consenting to the Participation in Clinical Trials
For the purpose of consenting to the participation in scientific research activities in clinical trials, the relevant provisions of Regulation (EU) No 536/2014 of the European Parliament and of the Council<ref>Regulation (EU) No 536/2014 of the European Parliament and of the Council of 16 April 2014 on clinical trials on medicinal products for human use, and repealing Directive 2001/20/EC should apply.