We have worked closely with MCRA since the summer 2010, relying on them to provide a full suite of clinical services to facilitate our study. These services include protocol writing and updates, IRB coordination, study monitoring, database management, statistics, and preparation of annual reports. MCRA provides a company of our size with the project management and clinical resources necessary to successfully run a clinical study in compliance with GCP and FDA regulations. We have been very pleased with the quality of support and timeliness of deliverables.





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