Aspire IRB was founded in 2004 by three women with many years of IRB experience, each one passionate about IRB work. Under their leadership, Aspire grew considerably while developing a reputation for distinction, professionalism, and integrity. Aspire IRB has an outstanding compliance history. In December, 2012 the United States Food and Drug Administration (FDA) audited Aspire IRB. The FDA categorized the audit as No Action Indicated, a perfect audit result.
Since 2008, Aspire has been fully accredited by AAHRPP. Aspire is committed to overseeing quality research and to protecting research participants. We strive to build lasting client partnerships through timely, efficient service and open communication.
The Aspire staff is knowledgeable about all applicable IRB laws and regulations. We promote a culture of excellence. Each Aspire staff member is dedicated to making a difference through ethical research. We employ quality controls to ensure each project is completed without error. You will find us to be flexible, responsive, and conscientious. We look forward to partnering with you.
The Principles We Built Our Business On
Aspire IRB appreciates the role that each individual plays in the IRB process, and continually supports those roles through team input, client communication, and community commitment.
Protecting People, Empowering Research, at Aspire IRB the difference is Service. Our team of dedicated IRB professionals will partner with you to successfully execute your clinical study. Fully AAHRPP accredited we have experience and expertise to review your Biological, Device, or Pharmaceutical study.
We built our customer portal ASAP to make managing large multicenter studies easy. ASAP remembers the sites you use in your studies, so adding a site to your study is just a mouse click away. Built-in Site, Start-Up, and Continuing Review reports help you manage critical phases of your large multicenter studies. ASAP is powerful in its search, export, print, and save functions, so you can easily access and use your study data and use it the way you want.
IRB Services are just one part of an Institution’s Human Research Protection Program. Aspire IRB offers a full range of services to help you manage your Institution’s IRB Services. From acting as a Central IRB for a single study, or providing administrative and electronic portal services for your Institution’s IRB, to outsourcing all of your IRB Services to Aspire IRB, we have a solution that meets your needs. To discuss a solution that meets your Institution’s needs contact us to setup an appointment.
Aspire IRB has extensive experience reviewing Phase I and Single Site submissions. You will work with a dedicated Project Lead who will act as an extension of your team and provide you a single point of contact. Your Project Lead will coordinate an administrative and scientific pre-review of your study to ensure our Board has all of the information it needs to evaluate your study.
Quick turnaround times keep your study on track with Initial Reviews completed in 6 to 8 business days, patient materials in 24 hours, and revisions within 3 business days.