A Paradigm Shift Towards Patient Involvement in Medicines Development and Regulatory Science: Workshop Proceedings and Commentary

Author:

Borup Gitte,Bach Karin Friis,Schmiegelow Merete,Wallach-Kildemoes Helle,Bjerrum Ole Jannik,Westergaard Niels

Publisher

Springer Science and Business Media LLC

Subject

Pharmacology (medical),Public Health, Environmental and Occupational Health,Pharmacology, Toxicology and Pharmaceutics (miscellaneous)

Reference31 articles.

1. Pushparajah DS, Geissler J, Westergaard N. EUPATI: collaboration between patients, academia and industry to champion the informed patient in the research and development of medicines. Journal of Medicines Development Sciences. 2015;1(1):74–80.

2. Hoos A, Anderson J, Boutin M, et al. Partnering with patients in the development and lifecycle of medicines: a call for action. Therapeutic Innovation & Regulatory Science. 2015.

3. European Medicines Agency. The patient’s voice in the evaluation of medicines: how patients can contribute to assessment of benefit and risk. 2013. http://www.ema.europa.eu/. Accessed September 14, 2015.

4. Tufts Center for the Study of Drug Development. Cost to develop and win marketing approval for a new drug is $2.6 billion. Tufts Center for the Study of Drug Development Web site. http://csdd.tufts.edu/news/complete_story/pr_tufts_csdd_2014_cost_study. Published November 18, 2014. Accessed September 14, 2015.

5. Smits RE, Boon WP. The role of users in innovation in the pharmaceutical industry. Drug Discov Today. 2008;13(7):353–359.

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