Tufts CSDD eBooks
Tufts CSDD eBooks, the newest additions to our publication catalogue, are comprehensive compendia of Tufts CSDD research findings. Offered in long-form digital format for mobile or desktop consumption, Tufts CSDD eBooks provide timely and highly relevant e-reference materials to inform the research-based pharma and biotech industry, as well as other stakeholders involved in new medicines development.
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Current Tufts CSDD eBook offerings:
UPDATED EDITION - FDA Trends: Path to Approval
Editor: Dr. Christopher-Paul Milne, Director of Research, Tufts Center for the Study of Drug Development
The FDA Trends: Path to Approval eBook is a comprehensive compilation of recent Tufts CSDD presentations and publications, government data, and expert perspectives related to FDA approval trends. Offered in long-form digital format for mobile or desktop consumption, the eBook covers a broad range of topics, including FDA expedited review programs, the global marketplace, benefit/risk, regulatory science, and differential impact of FDA workload on therapeutic areas.
NEW 2014 - 2015 UPDATE, including:
- New figures for R&D costs, approval time and success rates
- Tracking Ebola R&D over the last decade
- Biosimilars are “coming to America”
- Breakthrough Therapy Designation (BTD) impacts
- Trends in personalized medicine investment from 2010 to 2015
TABLE OF CONTENTS:
Here’s what reviewers are saying about Tufts CSDD’s FDA Trends eBook:
- "An excellent reference for medical and regulatory affairs teams.
- "Offers valuable insights into regulatory processes and trends."
- "Great overview of pertinent topics."
The FDA Trends eBook is also available in a multi-user license, giving everyone in your organization immediate access. Email us for pricing information.
PLEASE NOTE: Orders are processed as quickly as possible during Tufts CSDD business hours of 9AM – 5PM. Orders placed outside of business hours or on weekends will be processed and delivered at the on the following business day.
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|Tufts CSDD eBooks||$129|