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they are unfortunately in Europe theres not just one con since there are several ones they have different legal basis and they have have different legal traditions one of them is the concept of consent into data processing another one is the concept of consent into the treatment and the third one is the concept of constant into the research undertaken and those three concepts are similar but they are not identical and researchers doing research with medical information therefore need to be in line with all three concepts I think the most important argument is that you need to be in control of your information in order to be able to build trust on what happens with your data and putting you into the control for allowing you to build up trust needs your knowledge on whats going on and your agreement on whats going on when it comes to inform constant and medical research there is another reason for this because theres a very long and very important tradition also in medical law that f
