Buy ASME NQA Quality Assurance Requirements For Nuclear Facility Applications from SAI Global. ASME NQA-1– (Revision of ASME NQA-1–). Quality. Assurance. Requirements for. Nuclear Facility. Applications. AN AMERICAN NATIONAL. American Society of Mechanical Engineers (ASME) NQA (95 addenda) and editions. The requirements of these documents shall be complied with .

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Winchester Subcommittee on Assessment and Verification T.

PD635 ASME NQA-1-2008/1A-2009 Quality Assurance

Procurement document review shall be performed by personnel who have access asmf pertinent information and who have an adequate understanding of the requirements and intent of the procurement documents. Cursory supervisory reviews do not satisfy the intent of this Standard. A significant condition adverse to quality is one that, if uncorrected, could have a serious effect on safety or operability. Such documents shall include or be supplemented with appropriate criteria from para.

If necessary, an evaluation shall be made to determine the cause of the unacceptable cleanness and the actions required to preclude recurrence.

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Maintenance of Installation Cleanness. Known problems affecting the standard or previously proved designs and their effects on other features shall be considered. Measuring and test equipment shall be used and calibrated in hqa-1 that are controlled to the extent necessary to ensure that the required accuracy and precision are maintained.

Lead Auditors who fail to maintain their proficiency for a period of 2 years or more shall require requalification. McIntyre, Vice Chair N. Participation by federal agency representative s or person s affiliated with industry is not to be interpreted as government or industry endorsement of this code or standard. State what it is believed that the Standard requires.


Quality — Columbia Energy and Environmental Services

Quality assurance records shall be identified, generated, authenticated, and maintained, and their final disposition specified. The tests performed shall obtain the necessary data same sufficient accuracy for evaluation and acceptance. Calibration shall be against and traceable to certified equipment or reference standards having known valid relationships to nationally recognized standards, or to international standards known to be equivalent to and verified against corresponding nationally recognized standards.

Configuration items shall be maintained nqz-1 configuration management until the software is retired. Upon Purchaser acceptance of source verification, documented evidence of acceptance shall be furnished to the receiving destination of the item, to the Purchaser, and to the Supplier.

Nonconformances to design requirements dispositioned use-as-is or repair shall be subject to design control measures commensurate with those applied to the original design. Control of Special Processes. The work activities include but are not limited to managing, planning, siting investigation, design, computer software utilization, procurement, fabrication, manufacturing, installing, inspecting, testing, operating, and decommissioning.

To minimize the possible adverse effects of halogens, the chemical requirements for water used on components or systems containing austenitic stainless steel or corrosion-resistant alloy shall be as determined by technical evaluation. Definitions generic to quality assurance activities are included in Part I, Introduction, sectionTerms and Definitions.

The Standard focuses on the achievement of results, emphasizes the role of the individual and line management in the achievement of quality, and fosters the application of these requirements in a manner consistent with the relative importance of the item or activity.


American Aeme of Mechanical Engineers, Inc. Moreover, ASME does not act as a consultant for specific engineering problems or for the general application or understanding of the Standard requirements. The results of design verification shall be documented with the identification of the verifier clearly indicated. From Wikipedia, the free encyclopedia.

An does not pre-qualify or exempt an organization from a qualification audit being performed 208 the Purchaser of the items or services provided by the organization. The organization shall establish and implement processes to detect and correct quality problems. Design adequacy shall be verified by individuals other than those who designed the item or computer program. These procedures shall include the responsibilities and authority of the organizations whose functions affect the configuration of the facility including nwa-1 such as operations, design, maintenance, construction, licensing, and procurement.

Prospective Lead Auditors shall pass an examination that shall evaluate comprehension of and ability to apply the body of knowledge identified above. Requirement 11 Test Control. An inquiry letter concerning unrelated subjects will be returned.

Special process instructions shall include or reference procedure, personnel, and equipment qualification requirements. Where the design has been subjected to a verification process in accordance with 208 Part Part Ithe verification process need not be duplicated for identical designs.