J
James Mittra
Researcher at University of Edinburgh
Publications - 36
Citations - 432
James Mittra is an academic researcher from University of Edinburgh. The author has contributed to research in topics: Health care & Context (language use). The author has an hindex of 11, co-authored 36 publications receiving 384 citations.
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Life Science Innovation and the Restructuring of the Pharmaceutical Industry: Merger, Acquisition and Strategic Alliance Behaviour of Large Firms
TL;DR: It is suggested that mergers, acquisitions and strategic alliances represent a cluster of related activities that provide various strategic options for managing innovation and productivity deficit.
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Twenty-first century bioeconomy: Global challenges of biological knowledge for health and agriculture
TL;DR: In this article, an analysis of contemporary and future understandings of the bioeconomy using a co-evolutionary and interactive approach to examine the extent to which it may be different from other technological transformations is presented.
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Identifying viable regulatory and innovation pathways for regenerative medicine: a case study of cultured red blood cells.
TL;DR: A case study analysis of a project to derive red blood cells from human embryonic stem cells is described, including the systemic challenges arising from the selection of appropriate and viable regulatory protocols and technological constraints related to stem cell manufacture and scale up to clinical Good Manufacturing Practice (GMP) standard.
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Evolution of Business Models in Regenerative Medicine: Effects of a Disruptive Innovation on the Innovation Ecosystem.
TL;DR: The needs for more systemic analyses of the needs of potentially disruptive innovations, in RM and more widely, are highlighted and for policymakers to give greater attention to these insights in planning regulatory and other supporting initiatives, with the promotion of innovation in mind.
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Analysing stratified medicine business models and value systems: innovation-regulation interactions.
James Mittra,Joyce Tait +1 more
TL;DR: Two convergence models for co-development of a therapy and diagnostic before market authorisation are explored, highlighting the regulatory requirements and policy initiatives within the broader value system environment that have a key role in determining the probable success and sustainability of these models.