We use cookies to distinguish you from other users and to provide you with a better experience on our websites. Close this message to accept cookies or find out how to manage your cookie settings.
To save content items to your account,
please confirm that you agree to abide by our usage policies.
If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account.
Find out more about saving content to .
To save content items to your Kindle, first ensure [email protected]
is added to your Approved Personal Document E-mail List under your Personal Document Settings
on the Manage Your Content and Devices page of your Amazon account. Then enter the ‘name’ part
of your Kindle email address below.
Find out more about saving to your Kindle.
Note you can select to save to either the @free.kindle.com or @kindle.com variations.
‘@free.kindle.com’ emails are free but can only be saved to your device when it is connected to wi-fi.
‘@kindle.com’ emails can be delivered even when you are not connected to wi-fi, but note that service fees apply.
In order to gain allegiance, a transnational regulatory regime must be able to demonstrate its ‘regulatory legitimacy’ – it must persuade its members, and sometimes the global community in general, that it is addressing a true regulatory need. Most commonly, such regimes will appeal to one or more of the following conditions as being the basis for its regulatory legitimacy: transnational interdependency; global convergencies that are resulting in common regulatory needs that are more efficiently addressed at the transnational level; cosmopolitanism; the distinct concerns of particular transnational regional or professional populations; and the capacity of transnational law to facilitate emancipation from oppressive domestic regulatory structures. Establishing these various ‘bases of regulatory legitimacy’ often involve making empirical claims that can be subject to considerable contestation. As examined later in this volume, all this implicates the particular kinds of regulatory activities (see Chapter 3) and governance structures (see Chapter 4) the regime can support.
Taking a lead from Graeme Laurie’s willingness to ‘think outside the box’ – typified by his more recent work on ‘liminality’ – this chapter has as its thrust the idea that medical jurisprudence needs to speak to more than the leading cases and the nice doctrinal questions. It also needs to get the regulatory environment right for the upcoming technological developments – in genetics, robotics, additive manufacturing, nanotechnologies, artificial intelligence,, machine learning etc. – that promise to transform medical practice. Following this line of argument, medical lawyers should think outside the box of Law 1.0, where traditional legal principles, concepts and precedents are applied to new technologies and novel applications; engage with the regulatory challenges, including the challenges of regulatory connection and effectiveness but particularly that of regulatory legitimacy, that are the subject of Law 2.0 thinking; and join the embryonic Law 3.0 conversation, which contemplates not only smart technological solutions to regulatory problems but also humans being taken out of the loop (as both regulators and regulatees).
Recommend this
Email your librarian or administrator to recommend adding this to your organisation's collection.