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dc.contributor.authorCorbett, M
dc.contributor.authorWebster, A
dc.contributor.authorHawkins, Robert E
dc.contributor.authorWoolacott, N
dc.date.accessioned2017-04-19T16:58:14Z
dc.date.available2017-04-19T16:58:14Z
dc.date.issued2017-03-08
dc.identifier.citationInnovative regenerative medicines in the EU: a better future in evidence? 2017, 15(1):49 BMC Meden
dc.identifier.issn1741-7015
dc.identifier.pmid28270209
dc.identifier.doi10.1186/s12916-017-0818-4
dc.identifier.urihttp://hdl.handle.net/10541/620255
dc.description.abstractDespite a steady stream of headlines suggesting they will transform the future of healthcare, high-tech regenerative medicines have, to date, been quite inaccessible to patients, with only eight having been granted an EU marketing licence in the last 7 years. Here, we outline some of the historical reasons for this paucity of licensed innovative regenerative medicines. We discuss the challenges to be overcome to expedite the development of this complex and rapidly changing area of medicine, together with possible reasons to be more optimistic for the future.
dc.language.isoenen
dc.rightsArchived with thanks to BMC medicineen
dc.titleInnovative regenerative medicines in the EU: a better future in evidence?en
dc.typeArticleen
dc.contributor.departmentCentre for Reviews and Dissemination, University of York, Heslington, York, YO10 5DDen
dc.identifier.journalBMC Medicineen
refterms.dateFOA2018-12-17T14:54:26Z
html.description.abstractDespite a steady stream of headlines suggesting they will transform the future of healthcare, high-tech regenerative medicines have, to date, been quite inaccessible to patients, with only eight having been granted an EU marketing licence in the last 7 years. Here, we outline some of the historical reasons for this paucity of licensed innovative regenerative medicines. We discuss the challenges to be overcome to expedite the development of this complex and rapidly changing area of medicine, together with possible reasons to be more optimistic for the future.


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