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Q&A with the NCBIO Clinical Research Forum panel explores clinical trial barriers 

The panel at the NCBIO Clinical Trials Forum comprised moderater Abby Emanuelson, IQVIA's Erin Finot, Ultragenyx's Julie Harrell and Thermo Fisher Scientific's Rose Blackburne, M.D.

An expert panel explored the current state of clinical trial participation at the NCBIO Clinical Research Forum held Tuesday, Nov. 29. Panelists talked about ways to lower the barriers that stop patients from participating in clinical trials and discussed strategies for achieving diversity. They also explored the role of patient advocates and gave special consideration to efforts focused on rare diseases. 

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2022 NCBIO Year in Review

In this past year, we emerged from the isolation of COVID-19 thanks in no small part to the heroic work of the life sciences industry in developing vaccines, rapid tests and new treatments that have made the pandemic much more manageable. In spite of this success, we have faced tremendous pressure at the federal level with threats to intellectual property, the lifeblood of the industry, and a push to insert price controls with potential repercussions on innovation.

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