DIA: Driving Insights to Action
Science:Life Sciences
Medical Affairs professionals in India work in uniquely challenging, constantly changing clinical research and clinical practice landscapes. “They walk on a tightrope with that balance between what the company needs and at the same time what is acceptable in the eyes of the medical community,” explains Dr. Viraj Suvarna, an independent consultant and expert in medical affairs in India who served on the faculty for DIA India’s Crafting Sound Medical Affairs Professionals 2018 workshop, in this Global Forum podcast.
Analyzing Innovation’s Progress in Gottlieb Era
Comparing Generic Safety Profile with Branded Cousin
Defining Unmet Need Critical to Determining Value
Triple-A RWE: Adequate Data, Appropriate Designs, Actionable Evidence
US REMS Requirements for NDAs and BLAs
Epoietin Biosimilars: Qualitative Study of Patients' Views
Disparities Between FDA/EMA Review Processes
DIA Japan's Focus in Fall 2018
FDA Leadership on Future Biologics and EMA/FDA Cooperation
Global Perspectives on Patient Engagement
DIA Board Chair Discusses DIA Now and Digital Tomorrow
Integrating Genetic Medicine into Clinical Care
Regulatory Landscape of Drug-Device Combination Products
Value-Based Assessment & Contracting: What Needs to Be Done?
Block Chain, AI, Internet of Things: Future of PharmaTech?
“My Voice Needed to Be Heard”
IMEDS Collaboration Builds Upon Sentinel Surveillance
Statistical Strategies for Using Sources of Safety Data
Regulatory & Ethical Considerations in a Pediatric Trial
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