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control of dust and drafts, protection from extreme temperatures, and access to <br /> a source of stable power. <br /> Laboratories should be designed so that there is adequate separation of <br /> functions to ensure that no laboratory activity has an adverse effect on the <br /> analyses. The laboratory may require specialized facilities such as a perchloric <br /> acid hood or glovebox. <br /> Separate space for laboratory operations and appropriate ancillary support <br /> should be provided, as needed, for the performance of routine and specialized <br /> procedures. <br /> As necessary to ensure secure storage and prevent contamination or <br /> misidentification, there should be adequate facilities for receipt and storage <br /> of samples. The level of custody required and any special requirements for <br /> storage such as refrigeration should be described in planning documents. <br /> Storage areas for reagents, solvents, standards, and reference materials <br /> should be adequate to preserve their identity, concentration, purity, and <br /> stability. <br /> Adequate facilities should be provided for the collection and storage of <br /> all wastes, and these facilities should be operated so as to minimize environ- <br /> mental contamination. Waste storage and disposal facilities should comply with <br /> applicable federal , state, and local regulations. <br /> The location of long-term and short-term storage of laboratory records and <br /> the measures to ensure the integrity of the data should be specified. <br /> 4.2 EQUIPMENT/INSTRUMENTATION <br /> Equipment and instrumentation should meet the requirements and specifica- <br /> tions of the specific test methods and other procedures as specified in the <br /> QAPjP. The laboratory should maintain an equipment/instrument description list <br /> that includes the manufacturer, model number, year of purchase, accessories, and <br /> any modifications, updates, or upgrades that have been made. <br /> 4.3 OPERATING PROCEDURES <br /> The QAPjP should describe or make reference to all laboratory activities <br /> that may affect data quality. For routinely performed activities, SOPs are often <br /> prepared to ensure consistency and to save time and effort in preparing QAPjPs. <br /> Any deviation from an established procedure during a data collection activity <br /> should be documented. It is recommended that procedures be available for the <br /> indicated activities, and include, at a minimum, the information described <br /> below. <br /> ONE - 15 Revision 1 <br /> July 1992 <br />