Modern medicine development is not modern. It was simply the best we could do before the dawn of the digital age. This redesigns healthcare delivery, it will also redesign our conceptions of patient safety, medicinal product and medical devices development and clinical trials.
In this webinar – it will be explored what the increasing roll-out of modelling and simulation in healthcare could mean in terms of gaps in regulation, compliance and ethics. This webinar will be moderated by Peter O'Donnell (Brussels Correspondent, APM Health Europe / European Columnist, Applied Clinical Trials) and will include presentations from:
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Further information on the Avicenna Alliance can be found here