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How Regenerative Medicine Stakeholders Adapt to Ever-Changing Technology and Regulatory Challenges? Snapshots from the World TERMIS Industry Symposium (September 10, 2015, Boston).

Authors :
Bayon Y
Van Dyke M
Buelher R
Tubo R
Bertram T
Malfroy-Camine B
Rathman M
Ronfard V
Source :
Tissue engineering. Part B, Reviews [Tissue Eng Part B Rev] 2017 Apr; Vol. 23 (2), pp. 159-162. Date of Electronic Publication: 2016 Nov 21.
Publication Year :
2017

Abstract

Regenerative medicine (RM) is a fascinating area of research and innovation. The huge potential of the field has been fairly underexploited so far. Both TERMIS-AM and TERMIS-EU Industry Committees are committed to mentoring and training young entrepreneurs for more successful commercial translation of upstream research. With this objective in mind, the two entities jointly organized an industry symposium during the past TERMIS World Congress (Boston, September 8-11, 2015) and invited senior managers of the RM industry for lectures and panel discussions. One of the two sessions of the symposium-How to overcome obstacles encountered when bringing products to the commercial phase?-aimed to share the inside, real experiences of leaders from TEI Biosciences (an Integra Company), Vericel (formerly Aastrom; acquirer of Genzyme Regenerative Medicine assets), RegenMedTX (formerly Tengion), Mindset Rx, ViThera Pharmaceuticals, and L'Oreal Research & Innovation. The symposium provided practical recommendations for RM product development, for remaining critical and objective when reviewing progress, for keeping solutions simple, and for remaining relevant and persistent.

Details

Language :
English
ISSN :
1937-3376
Volume :
23
Issue :
2
Database :
MEDLINE
Journal :
Tissue engineering. Part B, Reviews
Accession number :
27771996
Full Text :
https://doi.org/10.1089/ten.TEB.2016.0292