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Medical Laboratories

US-A accredits medical laboratories to ISO 15189 and industry specific standards. This accreditation demonstrates to the marketplace and to regulators that the medical laboratories have met the US accreditation requirements and are periodically monitored for compliance.

US Accreditation for Medical Laboratories
  • Accredits third-party medical laboratories.

  • Assists medical laboratories develop a quality management system to ensure ISO/IEC 17025 and ISO 9001 requirements are met

  • Establishes inbuilt processes to educate laboratories to assess their own competence and personnel.

  • Assists in improving quality patient care, needs of patients and clinical personnel whom are responsible for the care of patients.

  • Increases health safety, confidentiality, ethical reporting practices and patient management.

  • The current US-A proposed scope available for applicant and accredited medical laboratories are as follows:

    • Clinical Biochemistry (sub-scope: Toxicology), Clinical Microbiology, Clinical Pathology, Genetics (sub-scope: Cytogenetics), Haematology, Histopathology [sub-scopes: Cytopathology (Cytology) Hospital Autopsy], Immunology, Medical Imaging, Molecular Pathology, Nuclear Medicine, Point-of-care Testing (POCT), Pharmacology
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