Julie Blasingim

CEO, Univo IRB

Julie Blasingim is a seasoned IRB executive with 20 years of extensive regulatory, operational, and compliance experience in human research protection and site operations of clinical research. She has served in a dozen senior leadership roles across multiple central IRBs including Independent IRB, Schulman, and Advarra. Julie is routinely consulted for her extensive human research protection regulatory expertise. She has hosted countless FDA inspections at both the IRB and under site operations and has managed multiple accreditations and certifications through AAHRPP and ISO.

Talk to Julie about these topics and more:

Human research protection regulations
Site operations of clinical research
Next-generations IRBs

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About Univo IRB

A next-generation institutional review board (IRB), unifying patients and research with a flexible, service-first approach. Univo IRB, formerly Principal IRB, is a next-generation institutional review board (IRB) specializing in the ethical review of Phase I-IV pharmaceutical, device, biologic, behavioral, and psycho-social research. We offer agile, expert solutions powered by modern technology and a service-first approach. Univo IRB holds accreditation through the Association for the Accreditation of Human Research Protection Programs (AAHRPP). With support from senior advisors and a leadership team with 60+ years of central IRB experience, Univo IRB guides your study forward while respecting the rights and welfare of patients every step of the way.

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