Welcome to the Blog

 Aspire continuously strives to elevate the quality of clinical trials by ensuring the safety of every human research participant. Our committed, CIP-certified team has over 45 years of IRB experience, and is focused on developing business relationships based on ethics, innovation and service. For research participants, that means a compassionate commitment to the highest levels of research protection. For our valued clients, it means accurate, expedited results and superior regulatory compliance.

We understand that completing IRB paperwork is an involved process, so we offer an integrated web portal for the access and management of your research and study data. Using our ASAP electronic system, multi-center CROs and sponsors can keep track of submitted documents, view scheduled IRB meetings, track missing information and retrieve approved site documents in a few clicks.

At Aspire, it's our mission to protect human subjects while developing a partnership with each client, and we demonstrate this resolution through our full AAHRPP accreditation. Endeavoring to deliver service excellence in all situations, we'll work hand-in-hand with you to bring critical, life-saving drugs and pharmaceutical innovation to the healthcare industry.

At Aspire, the difference truly is service. Together, we'll enhance quality of life through the promotion of ethical research and development.