Why Work With Us
Experience in clinical research
Wealth of experience in the clinical research related to all GCP related subject matters, trial management, site management, risk- based monitoring, quality management and coordination. Capabilities in management of Sponsor CRO relationships, CRO selection, management and oversight. Expertise in site management and clinical trial site management
We can provide consultancy in the area of the clinical evaluation process and reports for your medical device. Support in identifying the needs and potential gaps to meet the European Medical Device Regulation for clinical evidence, through either clinical investigations or Post Market Clinical Follow Up.