This in-person event is for professionals and stakeholders associated with newborn screening projects, such as the Generation Study, wanting to explore some of the challenges around balancing the benefits of extending screening for babies with rare conditions, with the involvement this requires from babies who do not stand to personally benefit.
Delegates should be ready to contribute constructively and as a part of the pragmatic discussions on newborn screening projects. As such, please email the hosts to ask about attending this invite-only event.
For more information on this event, including viewing its agenda, please visit its webpage or contact the event’s hosts, Centre for Personalised Medicine.
