Monitoring

Clients can hire our independent clinical trial monitoring services, from phase II to phase IV, whether in Spain or the rest of the world. Almost all of our BioClever CRAs (80%) are ACRP certified, and they all receive ongoing training in ICH and GCP Guidelines and internal SOPs.

Our annual staff turnover is low (less than 5%) and our employee satisfaction is high (90% of our people are happy and feel valued in their job*), so we can assure our clients that the same CRAs who start up a trial will be there at study-end.

All our CRAs are trained to anticipate site management issues and proactively develop and implement solutions. This approach is implemented from the earliest stages and throughout the clinical study, to ensure proper process flow and responsiveness. Most BioClever monitors are bilingual full-time employees, they are equipped with laptops and are always available by phone and e-mail when out of the office.

BioClever's study monitoring teams are recruited locally and based close to the sites they visit.

BioClever will take care of the following:

• Site selection
• Clinical trial and site management
• Monitoring visits
• Staff training
• Drug management
• Dedicated quality control
• Compliance
• Tracking of study milestones

*Anonymous survey conducted annually among BioClever's internal employees