Why the New Look?                    
800.431.9640
go
Capabilities > Phase lV / Post-Approval

Phase lV / Post-Approval


As regulatory requirements grow, Phase lV trials are becoming critical and costly stepping-stones to market release for drugs and medical devices. ClinicalRM's team is a proven solution to managing thousands of subjects in post-marketing studies to determine additional safety information, or pharmacovigilance, regarding the risks, benefits, and optimal usage of drugs and medical devices.

 
 
 
Corporate Headquarters
800.431.9640
330.278.2343


Federal Services Operations
301.620.1987

International Operations
800.431.9640
©2014, ClinicalRM, Inc.