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Advarra does not conduct its own clinical programs but provides regulatory review services and technology platforms that support thousands of active protocols annually. It serves as the IRB/IBC of record for major first-in-human studies—including mRNA vaccine trials—and helps accelerate study startup timelines while ensuring compliance and participant safety. Its platforms are widely adopted by leading academic centers, hospitals, CROs, pharma sponsors, and NCI-designated cancer centers[1][6].
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