Very well prepared CRAs to train site staff effectively. Leading to less protocol deviations, queries and good reliable data quality. CRAs support sites in an ongoing basis especially during FPI. Compared to other CROs, sites are not referred to a help desk.
Clinical Monitoring
Clinical monitoring with seasoned experts
Understanding Clinical Trials
Our Approach
CRAs support site team to deliver best possible performance
Start with extensive site training with focus on what is not part of the daily routine (e.g., PK samples, Diaries, Biopsy, Photography)
Provide convenient remote support during FPI
Ongoing and continuous close site staff support
Ongoing data cleaning
Timely reporting of PDs by CRA and review by PM and/or MM
Clinical Monitoring – Our Strategy
Always looking for the right strategy together with the sponsor
Risk-based monitoring
Remote Monitoring between Onsite visits
Remote Check of data with eCRF reports
Partial SDV (Data points to be monitored will be determined with sponsor after final protocol)
Approach can be customized to study and site needs and will be described in detail in monitoring manual
What we stand for
Strong connection of CRAs to site teams
Well trained and committed site teams
Excellent overview of CRA of site activities
Very good reachability of CRAs for site and sponsor
Ongoing sponsor oversight
Contact us now and receive more information about our capabilities
Our Services
We are a full-service CRO. We take this literally – whether you choose all or some of our service functions.
