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Amarex helps you to build a successful, defensible regulatory submission, while reducing time and saving you money.

AMAREX offers a full array of services to the pharmaceutical, biotech, medical device, and medical diagnostic development industries.


Services include:

• Phase I through IV Development Planning
• Protocol Development
• Global Investigator Identification
• Case Report Form Design
• Project Management
• Clinical Monitoring
• Data Management
• Statistical Analysis
• Site Auditing
• Regulatory Affairs
• Medical Writing
• Electronic Submissions
• Web-based Technology
• Data Safety Monitoring Committee
• FDA and other Regulatory Presentations
• FDA Advisory Panel Presentations

 

 


Amarex Clinical Research 2007