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I've tested storage of samples for detection test was, when 20 saved. As already mentioned, QC should be included measures RS in the individual tests, to check the tests. Control of the quality of the essential elements that must be performed to test during any one of these points.

It recognizes the systematic error. This can occur when a new batch of prove or changes made to the calibration of the device. These results are provided, so that the server, clinically relevant.

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A Laboratoryshould of clinical virology, so designed, that a minimal biological hazards to personal and public Thelaboratory and Thatcultures reduced protected against pollution. We have especially for clinical virology should;-there are 44 samples in 6 title, summarized most of which applies to all departments of pathology.

There are no formal meetings between senior test-laboratory personnel and management services, objectives and financing agreements as personal and direction of the respective order numbers Orclinical is carried out by a scientific consultant pathologist trained Staffwith are suitable.

There is one Ofaccountability line documented for the staff of the Chief of the Allunqualified of the staff should be monitored.

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Descriptions to all employees and all employees have a job Contractof would be regular and personal encounters regains a full induction program c. Facilities there are a total of 10 standard in this area.

Thisinclude offices and laboratories, space suitable for receiving and dealing with memory Andspecimen-Stafffacilities. There should be a sufficient lighting, heating, ventilation, and drainage of water and gas. A safe work Environmentmust be for security officer is responsible.

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There are Communicationfacilities, corresponding data storage and recovery. There are corresponding maintained Scientificequipment, which must be managed correctly.

Laboratory forms should Includeunique identity and support information for patients. Reportsshould is accurate, complete and clinically relevant include sufficient OfCollection, must be patient identities tests, time and date of the Declaration.

A recording of the material all reagents, calibration and quality control.

Should write protocols for each experience, contain the preparation of materials, reagents, such as the calculation of results and interpretation of the functioning of internal control. There is a written record for the Normalreporting and the oral report on the results. It should be also Beprotocols for maintenance, as well as the Thedecontamination of all items of equipment and construction. APolicy that describes that after hours of service must be started.

In hospitals, a consultant microbiologist named is responsible for institutional infection control. In addition, his personal rating must plan Anestablished. Clinical testing of the service Becontinually be carried out and Manager should regularly take part controls in other clinical disciplines.

Controls for each test should be within the framework of the validity of the tender criteria and the manufacturer of the acceptable results.

Normally, each test kit has a number of positive and Negativecontrol be included in each test. This Controlsare believes that internal controls, while all other Controlsincluded in the operation of external control are invoked.

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