Question: https://www.bmj.com/bmj/section-pdf/758916?path=/bmj/348/7964/Editorials.full.pdf what are the advantages and drawbacks of the EU's two-part approach to clinical trial review? Do you believe that Member States should have a

https://www.bmj.com/bmj/section-pdf/758916?path=/bmj/348/7964/Editorials.full.pdf

what are the advantages and drawbacks of the EU's two-part approach to clinical trial review? Do you believe that Member States should have a greater role in the risk-benefit assessment process? If so, what specific changes would you propose? If not, how would you respond to the concerns raised in the linked article?

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