Process Areas for CMMI ML2:

REQUIREMENTS MANAGEMENT (RM)

PROJECT PLANNING (PP)

PROJECT MONITORING AND CONTROL (PMC)

Supplier Agreement Management (SAM)

Measurement and Analysis (MA)

PROCESS AND PRODUCT QUALITY ASSURANCE (PPQA)

CONFIGURATION MANAGEMENT (CM)

PA: PROCESS AND PRODUCT QUALITY ASSURANCE (PPQA)

3 specific goals (SG) and 1 generic goal (GG)

SG1: Adherence of the performed process and associated work products and services to applicable process descriptions, standards and procedures is objectively evaluated.

Practice Goal & Practice Statements Document Evidence
SP 1.1 Objectively evaluate the designated performed processes against the applicable process descriptions, standards and procedures. ¡@
SP 1.2 Objectively evaluate the designated work products and services against the applicable process descriptions, standards, and procedures. ¡@

SG2: Noncompliance issues are objectively tracked and communicated, and resolution is ensured.

Practice Goal & Practice Statements Document Evidence
SP 2.1 Communicate quality issues and ensure resolution of noncompliance issues with the staff and managers. ¡@
SP 2.2 Establish and maintain records of the quality assurance activities. ¡@

GG2: The process is institutionalized as a managed process.

Practice Goal & Practice Statements Document Evidence
GP 2.1 (CO 1) Establish and maintain an organizational policy for planning and per-forming the process and product quality assurance process. ¡@
GP 2.2 (AB 1) Establish and maintain the plan for performing the process and product quality assurance process. ¡@
GP 2.3 (AB 2) Provide adequate resources for performing the planned process, devel-oping the work products and providing the services for the process and product quality assurance process. ¡@
GP 2.4 (AB 3) Assign responsibility and authority for performing the process, devel-oping the work products, and providing the services of the process and product quality assurance process. ¡@
GP 2.5 (AB 4) Train the people performing or supporting the process and product quality assurance process as needed.  ¡@
GP 2.6 (DI 1) Place designated work products of the process and product quality as-surance process under appropriate levels of configuration management. ¡@
GP 2.7 (DI 2) Identify and involve the relevant stakeholders of the process and prod-uct quality assurance process as planned. ¡@
GP 2.8 (DI 3) Monitor and control the process and product quality assurance process against the plan for performing the process and take appropriate corrective action. ¡@
GP 2.9 (VE 1) Objectively evaluate adherence of the process and product quality assurance process against its process description, standards, and procedures, and address noncompliance.  ¡@
GP 2.10 (VE 2) Review the activities, status, and results of the process and product quality assurance process with management and resolve issues. ¡@

Common features of the generic practices:

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