Clinical                  

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.

 

 

 

 

MCRA is not a law firm and neither provides legal advice to its clients nor can affirm the legal or regulatory validity of the materials of which it provides. MCRA recommends that its clients consult an attorney to discuss any legal issues that relate to its business and/or MCRA services