Risk Based Monitoring

 

Category: *CRO

Exhibitor: AMAREX TAIWAN, LLC

Booth No: M824

 

Characteristic

 

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

Services include:
1. Study Phase and Design
2. Program and Protocol Design
3. Clinical Monitoring
4. Medical Monitoring
5. Remote Monitoring
6. Data & Analysis Review
7. Primary and Secondary Study Objectives
8. Safety Profile of Product / Device
9. Complexity of Study-Specific Requirements
10. Study Duration
11. Site Management
12. Identify Critical Study Data and Processes
13. Perform a Risk Assessment to Identify Risks to Critical Data and Processes
14. Design a Monitoring Plan Tailored to Identified Important Risk

 

Other Products

 

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  Medical Writing

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  Regulatory Affairs

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  Pharmacovigilance

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  Biostatistics

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  Project Management

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  Clinical Site Feasibility

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  Data Management

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  Clinical Operations

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  Consulting Services

 

 

 

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