Achieve has the outstanding rapid start-up capabilities needed to expedite the clinical trial process. We can obtain approval and start clinical research studies within days of receiving final protocol. Our rapid start-up clinical trials are expertly coordinated by our dedicated sub-team who is committed to fast and efficient implementation with a focus on quality and accuracy.
Our rapid start-up capabilities are so advanced due to the large population of potential patients in the local areas where we are located. Achieve attracts a population of diverse demographics for our clinical trials. Our facilities are centrally located and easy to commute to and from for volunteers and patients alike.
We have profound experience in rapid start-up studies across a broad spectrum of conditions and sponsors. Our competencies in many different areas allow us to quickly launch trials with ease. We maintain a precise chain of custody for critical files and investigational drugs with our innovative and streamlined tracking system.
At Achieve, we have resources dedicated to the rapid receipt of regulatory approvals with Institutional Review Boards (IRBs). We also have efficient protocol implementation and organized training with principal investigators (PIs) and coordinators. Achieve is unmatched in our rapid start-up capabilities for clinical research trials.