Maintaining participant safety site consistency and data quality are some of the most important responsibilities of clinical trials. 

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Amarex's philosophy and strategy work alongside with the regulatory and industry guidelines and have lead to successful implementation in a variety of study designs and phases.

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Our collaborative approach allows Amarex and our clients to come up with resolutions that are the best study-specific monitoring strategy for their clinical trial.

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Services include:

• Study Phase and Design

• Program and Protocol Design

• Clinical Monitoring

• Medical Monitoring

• Remote Monitoring

• Data & Analysis Review

• Primary and Secondary Study Objectives

• Safety Profile of Product / Device

• Complexity of Study-Specific Requirements

• Study Duration

• Site Management

• Identify Critical Study Data and Processes

• Perform a Risk Assessment to Identify Risks to Critical Data and Processes

• Design a Monitoring Plan Tailored to Identified  Important Risk