Literature DB >> 19580404

Industry perceptions of barriers to commercialization of regenerative medicine products in the UK.

Anke C Plagnol1, Emma Rowley, Paul Martin, Finbarr Livesey.   

Abstract

AIMS: Regenerative medicine is an emerging field with the potential to provide widespread improvement in healthcare and patient wellbeing via the delivery of therapies that can restore, regenerate or repair damaged tissue. As an industry, it could significantly contribute to economic growth if products are successfully commercialized. However, to date, relatively few products have reached the market owing to a variety of barriers, including a lack of funding and regulatory hurdles. The present study analyzes industry perceptions of the barriers to commercialization that currently impede the success of the regenerative medicine industry in the UK. MATERIALS &
METHODS: The analysis is based on 20 interviews with leading industrialists in the field.
RESULTS: The study revealed that scientific research in regenerative medicine is thriving in the UK. Unfortunately, lack of access to capital, regulatory hurdles, lack of clinical evidence leading to problems with reimbursement, as well as the culture of the NHS do not provide a good environment for the commercialization of regenerative medicine products.
CONCLUSION: Policy interventions, including increased translational government funding, a change in NHS and NICE organization and policies, and regulatory clarity, would likely improve the general outcomes for the regenerative medicine industry in the UK.

Entities:  

Mesh:

Year:  2009        PMID: 19580404     DOI: 10.2217/rme.09.21

Source DB:  PubMed          Journal:  Regen Med        ISSN: 1746-0751            Impact factor:   3.806


  4 in total

1.  Regulation of stem cell-based therapies in Canada: current issues and concerns.

Authors:  Barbara von Tigerstrom; Thu Minh Nguyen; Bartha Maria Knoppers
Journal:  Stem Cell Rev Rep       Date:  2012-09       Impact factor: 5.739

2.  Perspectives on Challenges to Cell Therapy Development in Taiwan: Strengthening Evidential Standards and Ways Forward.

Authors:  Bilikis Aderonke Abolarinwa; Malissa Kay Shaw; Chung-Hsi Lee
Journal:  Front Bioeng Biotechnol       Date:  2021-12-16

3.  The Tissue-Engineered Vascular Graft-Past, Present, and Future.

Authors:  Samand Pashneh-Tala; Sheila MacNeil; Frederik Claeyssens
Journal:  Tissue Eng Part B Rev       Date:  2015-10-08       Impact factor: 6.389

4.  Challenges in Advanced Therapy Medicinal Product Development: A Survey among Companies in Europe.

Authors:  Renske M T Ten Ham; Jarno Hoekman; Anke M Hövels; Andre W Broekmans; Hubert G M Leufkens; Olaf H Klungel
Journal:  Mol Ther Methods Clin Dev       Date:  2018-10-11       Impact factor: 6.698

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.