Clearpoint Image Review Centre is an imaging CRO that provides sponsors with extensive medical, operational and image management expertise in support of clinical trials. Originally established in 1999, we bring you 23 years of experience in the field of planning and executing Independent Blinded Reads for regulatory clinical studies.
Our specialist team has successfully brought numerous clinical studies through US FDA and EU inspections with no major findings. Our method is based on proven SOPs adding value and speed to your clinical studies shortening your time to market.
WHAT WE OFFER
We offer cost-effective and flexible solutions ranging from simple image data handling tasks to global multi-modality multicentre trials. All our systems are validated (510k, GCP) and operate according to relevant regulations (GCP, HIPAA, 21 CFR part 11 etc.) and all services provided are GCP compliant.
An overview of our process
Our systems and processes are highly modular and can be selected in any combination.
Image collection and processing is available on-line with global access and real time tracking.
We offer full GCP compliance in a secure and controlled environment.