Aspire IRB in Santee, CA, is a leading provider of comprehensive solutions for study planning, site enablement, and ethical review services for sponsors, CROs, and research sites. With a focus on quality compliance, diversity, and inclusion, Aspire IRB offers a single source of expertise for protocol planning, data monitoring, and endpoint adjudication to help clients succeed in their clinical trials.
With a team of nearly 200 IRB experts and a vast clinical advisory network, Aspire IRB ensures swift determination of protocols and documents, with accelerated timelines for study reviews. Boasting 55 years of experience in independent ethical review, Aspire IRB is dedicated to upholding the highest standards of health and participant safety, making them a trusted partner in the research community.
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