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May 11, 2016: ”Pharma, Science, and Innovation: What Does the Future Hold for the Health Care Industry and for Patients?”
Jerry Avorn, The First Amendment and Pharmaceutical Promotion , Health Affairs Blog, March 11, 2016
Tufts Center for the Study of Drug Development, Tufts CSDD Assessment of Cost to Develop and Win Marketing Approval for a New Drug Now Published , Press Release, March 10, 2016
PhRMA (Pharmaceutical Research and Manufacturers of America), Policy Solutions: Delivering Innovative Treatments to Patients , March 2016
PhRMA (Pharmaceutical Research and Manufacturers of America), Prescription Medicines: Costs in Context , 2016
Jonathan J. Darrow, Jerry Avorn, & Aaron S. Kesselheim, New FDA Breakthrough-Drug Category – Implications for Patients , New Engl J Med 2014;370:1252-62 & 371:87-90
Aaron S. Kesselheim, et al., Trends in utilization of FDA expedited drug development and approval programs, 1987-2014: cohort study , BMJ 2015; 351:h4633
Aaron S. Kesselheim, et al., The Roles of Academic, Rare Diseases, and Repurposing in the Development of the Most Transformative Drugs , HEALTH AFFAIRS 34, NO. 2 (2015): 286–293
Jerry Avorn & Aaron S. Kesselheim, Perspective, The 21st Century Cures Act – Will It Take Us Back in Time? , New Engl J Med 2015;372:2473-5 & 373:1677-80
Aaron S. Kesselheim, et al., Characteristics of Clinical Trials to Support Approval of Orphan vs. Nonorphan Drugs for Cancer , JAMA.2011;305(22):2320-2326