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 QCR has extensive experience working with domestic and foreign governmental agencies and offices, as well as with international agencies such as USAID, WHO, UNAIDS, PAHO, and the World Bank. QCR has the experience communicating with outside regulatory, governmental, and scientific bodies to ensure that your trial will be well-coordinated.

Safety monitoring

Clinical monitoring

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