Research and Development: Productivity Assessment
A Panel Discussion Among Experts on R&D Productivity
Deliverables: Transcript
Study Description and Objectives
To assess the expected productivity, i.e. trends in successes, of the pharmaceutical/biotechnology pipeline in the next five years.
§ Determine the current state of pharmaceutical R&D and expected trends in the strength of the resulting pipeline
§ Assess factors contributing to the success rate of the R&D success
§ Determine where improvement possible:
o Discovery: in-licensing and partnerships
o Clinical trials completion
§ Use of validated surrogate endpoints; focus on personalized medicine
§ Adaptive trial design
§ Outsourcing to CROs, globally (e.g., Asia)
§ Technology, e.g., e-enabled technologies in the clinical research process
o Regulatory submission and approval: likelihood of the FDA policy changes, e.g., live licenses and the impact on R&D
o Manufacturing
o Marketing
§ Evaluate other issues potentially affecting R&D success:
o Changes in R&D models (e.g., focus on approval in stages versus blockbuster approvals; more focus on phase II trials, etc.)
Inclusion Criteria
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Inclusion Criteria
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§ Number of Panelists: 4-6 experts on R&D pipeline trends § Published on R&D and pipeline trends § Academic professional setting |
Hospitals Represented
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Institution |
State |
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IL |
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MA |
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MA |
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AZ |
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