MIL-PRF-38535L规定了集成电路或微电路的一般性能要求，以及采购时应满足的质量和可靠性保证要求。本规范的目的是让设备制造商能够灵活地最大限度地实施最佳商业实践，同时仍然提供满足军事性能需求的产品。详细要求、微电路的具体特性以及其他对特定用途敏感的规定将在设备规范中规定。本文概述的质量保证要求适用于制造线上建造的所有微电路，该生产线通过制造商的质量管理（QM）计划进行控制，并已由资格鉴定机构（QA）根据本文的要求进行认证和鉴定。 本规范提供了包括RHA在内的多个产品保证级别。本文中的认证和资格部分概述了合格制造商清单（QML）中列出的制造商应满足的要求。在QML上列出技术流程后，制造商应持续满足或改进所有QML产品的认证和合格程序、QM计划、制造商审查系统、状态报告以及质量和可靠性保证要求的既定基线。制造商可提出满足本规范要求的替代方法。这些替代方法将由资格认证机构批准。本规范要求制造商建立工艺流程基线。如果有足够的质量和可靠性数据可用，制造商可通过QM计划和制造商的审查系统修改、替换或删除试验。 有关QML过程及其原理的更多信息，请参见本文第6.5节。克拉斯。

MIL-PRF-38535L establishes the general performance requirements for integrated circuits or microcircuits and the quality and reliability assurance requirements, which are to be met for their acquisition. The intent of this specification is to allow the device manufacturer the flexibility to implement best commercial practices to the maximum extent possible while still providing product that meets military performance needs. Detail requirements, specific characteristics of microcircuits, and other provisions which are sensitive to the particular use intended will be specified in the device specification. Quality assurance requirements outlined herein are for all microcircuits built on a manufacturing line which is controlled through a manufacturer's quality management (QM) program and has been certified and qualified by the Qualifying Activity (QA) in accordance with requirements herein. Several levels of product assurance including RHA are provided for in this specification. The certification and qualification sections found herein outline the requirements to be met by a manufacturer to be listed on a Qualified Manufacturer Listing (QML). After listing of a technology flow on a QML, the manufacturer is to continually meet or improve the established baseline of certified and qualified procedures, the QM program, the manufacturer's review system, the status reporting, and quality and reliability assurance requirements for all QML products. The manufacturer may present alternate methods of addressing the requirements contained in this specification. These alternate methods will be approved by the Qualifying Activity. This specification requires a manufacturer to establish a process flow baseline. If sufficient quality and reliability data is available, the manufacturer, through the QM program and the manufacturer's review system, may modify, substitute, or delete tests. Additional information on the QML process and its philosophy is available in 6.5 herein. Clas.