June 9, 2022 9am-4:15pm
This year’s bioethics roundtable, our 12th!, is hosted by Deloitte and will focus on equity and social responsibility in the bio-pharmaceutical sector and debut our new Good Pharma Scorecard (GPS) rankings on diversity and fair inclusion in research.
When: June 9, 2022 – 9am-4:15pm ET
Where: Deloitte’s NYC Offices
October 19, 2022 — October 20, 2022
The National Health Council hosts its 2022 Science of Patient Engagement Symposium, From Research to Action: Health Equity for All. Over the past ears, the COVID-19 pandemic has upended the world and magnified health inequities among historically underrepresented racial/ethnic groups. The science of understanding the patient has never been more important. Health equity research, where diverse patients are at the core of scientific inquiry, is imperative to tackling inequities. BEI’s Founder, Jennifer E. Miller, PHD, will Keynote on Trust in Medical Research.
June 9, 2022 9am-4:15pm
This year’s bioethics roundtable, our 12th!, is hosted by Deloitte and will focus on equity and social responsibility in the bio-pharmaceutical sector and debut our new Good Pharma Scorecard (GPS) rankings on diversity and fair inclusion in research.
When: June 9, 2022 – 9am-4:15pm ET
Where: Deloitte’s NYC Offices
September 21, 2020 1:00PM-2:15PM EDT
ISPOR and the Innovation and Value Initiative (IVI) are collaborating—with help from an expert advisory committee—to define a series of dialogues that highlight key challenges confronting HEOR methodologists, patients, clinicians, and policy-makers during the COVID-19 pandemic. The webinar series will explore multiple viewpoints and focus on potential pathways for solutions in international and U.S.-focused health technology assessment and value assessment (VA/HTA).
June 23, 2019 — June 27, 2019
Panelists will explore the pros and cons of the pathway from the patient perspective and learn about how regulators and sponsors may help facilitate the development of critically needed treatments. This discussion will introduce a streamlined approach to early-stage development of therapies to address severely debilitating or life-threatening diseases and consider the potential value of a global regulatory approach.
Location: San Diego, CA
June 5, 2019 — June 7, 2019
Dr. Jennifer E. Miller answers “Whose Data Is It” question.
This 75-minute session will look at the ethical considerations, legal aspects, coaching perspectives and athletic viewpoints related to ownership of sports biometric data. This session will be moderated by Jeremy Abbate from Scientific American.
Location: Columbus, Ohio
September 16, 2019 — May 16, 2019
In June 2019, Cambridge University Press published Transparency in Health and Health Care in the United States, a volume, edited by Holly Fernandez Lynch, I. Glenn Cohen, Carmel Shachar, and Barbara J. Evans, with a chapter on clinical trial transparency and data sharing by Jennifer Miller (Founder of Bioethics International and an Assistant Professor at Yale) stemming from Harvard’s Petrie-Flom Center’s 2017 conference, on this health policy buzzword, recognizing its true limitations, so that transparency can be utilized as a solution to pressing health policy issues. Jennifer E. Miller will speak on a panel with Glenn Cohen and Holly Fernandez Lynch
