The QA division of ChemDiv’s clinical research division, IPharma, is highly experienced in vendor, site, CRO, and drug depot audits. Each of the trials that we conduct undergoes independent audit whether an audit has been included in the study budget or not. Our QA team implements effective training and crafts SOPs compliant with GCP and ICH regulations. We conduct regular co-monitoring visits with our CRAs, and verify case report forms to ensure that trials are conducted to very high quality standards.
Please contact our team at [email protected] to discuss your specific needs and application.