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Quality Management

Quality Improvement is an ongoing goal and is at the core of our operating philosophy. Identifying and developing programs to continuously improve quality are the first steps. This is followed by implementing key metrics that enable the monitoring and reporting of results. Cambridge Biomedical's Quality Assurance (QA) staff combines scientific expertise with a deep knowledge of FDA, GLP, CLIA and CAP regulations to maintain the highest standards.

Clinical Quality Assurance's internal quality systems are designed to allow Cambridge Biomedical to meet or exceed its obligations to both customers and regulatory authorities.

Our programmatic approach enables Cambridge Biomedical to anticipate the information that clients will require. QA systems are built into the projects that provide information in a user compatible form.

Talk to Us about Key Quality Areas:

• Quality Manual
• Document Control System
• Training Programs
• Proficiency Testing
• Competency Testing
• Department Specific Quality Metrics
• Vendor Selecting and Auditing
• Computer and System Validation
• Assay Validation Procedures