Quality Assurance

About CLP

Clinical Laboratory Partners' quality management system actively monitors quality performance indicators for the entire process of laboratory services, from laboratory specimen collection and analysis to reporting, and billing. Performance improvement initiatives are measured through customer and employee surveys, and self-assessment. These indicators become the driving force behind the active quality improvement program. All indicators and activities are closely supervised by senior management.

Corporate Integrity

Clinical Laboratory Partners, LLC is committed to compliance with all applicable State and Federal guidelines as applies to laboratories. This includes, but not limited to, Clinical Laboratory Improvement Act (CLIA), the Centers of Medicare & Medicaid Services (CMS) and the HIPAA Privacy regulations. CLP administers policies throughout its organization to ensure compliance is maintained. Strict adherence to our code of ethics and conduct not only ensures our employees are ethical in everything they do, but our business partners as well.

Safety

All specimens will be handled using universal precautions. Every effort will be made to protect all health care workers from exposure to human immunodeficiency viruses (HIV) and the hepatitis viruses. CLP's Safety Policies adhere to federal requirements, including OSHA provisions.


Main Facility - 129 Patricia M. Genova Drive, Newington, CT 06111 - (800) 286-9800
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