DIA: Driving Insights to Action
Science:Life Sciences
Dr. Susan Forda serves as Vice President of International Regulatory Affairs for Eli Lilly & Company Limited in the UK. She also contributes her expertise to various committees for the European Federation of Pharmaceutical Industries and Associations (EFPIA) and will serve as Co-Chair for DIA’s EuroMeeting 2017. In this interview with DIA Global Forum Editor Dr. Alberto Grignolo, Dr. Forda explains her perspective on health care and regulatory challenges facing Europe and on the EuroMeeting theme, From Bench to Bedside and Back. “This theme is really important at this juncture because we know that patients are increasingly taking an active role in their health care, and this connectivity is enabled by rapid improvements in technology – for instance, through the immediate availability of credible information in the palm of our hands,” she suggests. “The patient can provide access to knowledge that no one else does.” To learn more, register for our DIA EuroMeeting 2017 in Glasgow!
Innovative Partnering Models and Outsourcing Strategies
Innovative Approaches to Ensuring Quality in Clinical Trials and Compliance to Good Clinical Practice (GCP)
Trends in Pharmaceutical Quality
Innovative Technology in Clinical Development
Interview with DIA Annual Meeting Co-Chair Dr. Michael Rosenblatt
Innovation in Vaccine Development
Implementing Innovation- Globally Conducive Regulatory Policies
Availability of Medicinal Products: Drug Shortages
Medical Devices and Combination Products
Pharmacovigilance in 2015- Poised for convergence of innovation
Spiros Vamvakas on Early Dialogue with Regulators
Detlef Niese on Translational Medicine
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