DIA: Driving Insights to Action
Science:Life Sciences
Dr. Hans-Georg Eichler, Senior Medical Officer of the EMA, EU, will co-chair Theme 2, Innovation of Health Care Product Development – What Are the Key Success Factors?, at our DIA EuroMeeting 2017 in Glasgow, Scotland. “Over time, we have realized that regulators also have a role in supporting innovation,” he explains. “They’re not just gatekeepers – they’re also enablers.” In this exclusive podcast, Dr. Eichler overviews the impact of the Clinical Trial Regulation on therapeutic innovation, how patients and payers might contribute to such innovation, and the opportunities and challenges ahead, in Europe. “The barriers, as usual, are our own conservativism and difficulty in letting go of all of our usual ways,” he suggests. Register for DIA EuroMeeting 2017 in Glasgow!
Relevance Will Put Europe on Investment Fast Track
Risk Inherent in Benefits of Drug/Device Products?
EU Business and Data Needs Converge Through Telematics
RIM Accelerating Efficiencies in Regulatory Pathways
Translating Clinical Trials into Clinical Benefit
More Tools & Data Sources: More Insights for RBM?
Landmark AMA to Rely on Regulatory Reliance
Healthy Population Key to Economic Success
Defining Rational Medicine and Research at DIA Japan 2019
How Do You Put Your Disease on the Agenda?
Participatory Medicine Changing Information Exchange
New Ethics and Consent Guidelines Pillars for Safety in India
Real World Data Expanding into Label Expansion
Educating Persons Critical in Personalized Medicine
FDA Payer Communication Guidance Steps Toward Sustainability
Genetic Engineering Transforming Research Ethics
Only Big Trust Propels Big Data into Big Discoveries
Empowering Today’s Patients to Help Tomorrow’s
Imaging Data Plus AI “One of the Best Combinations”
Clinical Trial Diversity Begins (and Ends) with Patients First
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