A stronger site means more studies and better sponsors
For sites already running studies, we build the processes that get them considered more often and for more substantial protocols. How many studies a site receives follows from how it operates.
Professional development
Experience of working to international protocols, alongside established sponsors and investigators.
Early access to investigational products
Experience with medicinal products before they enter current treatment guidelines.
Scientific recognition
Authorship in publications, and standing among peers and in the professional community.
Transparent remuneration
Payment for investigator work on transparent terms, in line with the study protocol.
The processes on which site selection turns
GCP compliance and quality at site level are the first matters a sponsor or CRO examines when deciding whether to place a protocol.
Standardised processes
Procedures are made uniform, so that recruiting or replacing staff does not affect how the site performs.
Routine work automated
Manual work is removed: temperature monitoring, logs, reminders and reporting.
Visibility in the professional community
We make the site and the investigator known to sponsors, CROs and peers, so that you are considered when protocols are allocated.
Worked as a sub-investigator and ready to open a site of your own?
We will help build a research site from the beginning: processes and SOPs, documentation, the ethics committee, staff training and full support through to the first study.
Tell us about the facility and we will say where to start
A short call commits you to nothing. After it you will know the scope of the work and its cost, even if you decide to do everything in-house. We reply within one working day.