The need for proportionate regulation of clinical trials
Ces deux articles analysent la controverse suscitée par une directive de l'Union Européenne sur la réglementation des essais cliniques
In a draft report about the upcoming European Union Data Protection Directive, the European Parliament Committee on Civil Liberties, Justice and Home Affairs suggests, by contrast with the position of the European Commission, that processing of data for scientific reasons should not be exempt from strict requirements of specific consent by research particpants. The committee's amendment is an example of how the regulatory framework for the protection of human research participants seems not to k ...
The Lancet Oncology , commentaire, 2012