Alquest services: Clinical monitoring for medical device firms
Alquest is widely recognized for its high-quality clinical monitoring services for medical device studies.
Alquest-monitored clinical sites have withstood FDA inspection during our 16 years in business.
- Alquest clinical monitors, who double as CRAs, understand the larger context of the monitoring effort
- When authorized, our clinical monitors are capable of resolving discrepancies on site
- Our goal is to elevate site compliance, not assign fault
- Our clinical monitors average 10.5 years of experience in the device industry, and 3.9 years of tenure with Alquest
Alquest directly employs highly professional clinical monitors who are skilled at helping clinical sites yield valid, FDA-acceptable clinical data. Alquest monitors are clinical professionals who understand both GCP requirements as well as entire clinical continuum from sponsor, site and FDA perspectives. Our monitors’ ultimate goal is to elevate site performance and morale, not to assign fault or blame. Alquest monitors also remain in close communication with our data management/statistical staff to identify and head off potential problems.





