Clinical research infrastructure development

Research site assessment and preparatory study development

Strategic consulting

Project management for research site coordination and oversight

Liaison with industry, government and other institutions

Safety monitoring

Clinical monitoringQCR staff can provide diligent and efficient monitoring to ensure adherence to GCP/ICH guidelines for licensure-driven clinical trials. We have vast domestic and international experience monitoring in the field as well as internally within sponsor companies. Our expertise and attention to detail will help you identify problems during the course of monitoring so that you can be assured that your data will be clean and complete by study closure.

Development of research plans and reports including proposals, timelines, protocols, consent forms, CRFs, SOPs

Medical writing

Preparation of presentations to IRBs, DSMBs, FDA, and other international institutions

Training for research coordinators and monitors

Access to well-trained and experienced investigators