ChemDiv chemistry of cures

In order to assure that all projects are conducted under the highest quality, ChemDiv utilizes an independent quality assurance group to audit projects and train our clinical staff.  SOPs are compliant with ICH and GCP and regulatory requirements.  We conduct regular co-monitoring of CRAs as well as data management (EDC) verification to maintain high and consistent monitoring.

Find attached:

ChemDiv-Clinical_Development.pdf

see also:

Clinical Trial Management
Clinical Trial Monitoring
Late Stage Research Services