Statistical Process Monitoring (SPM) Checklist
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Process Definition & Identification
Ensures the process being monitored is clearly defined and its critical characteristics are understood.
Process Description
Process ID / Code
Process Type (e.g., Machining, Assembly, Coating)
Critical Process Parameters (CPPs)
Process Input Materials/Components
Target Value (for key CPP)
Potential Process Risks/Variability Sources
Data Collection & Recording
Focuses on the accuracy, reliability, and completeness of data being collected for process monitoring.
Sample Size (n)
Sampling Frequency (Units/Time)
Data Point Interval (Time)
Data Source
Description of Data Collection Equipment
Units of Measurement
Data Validation Procedures (e.g., range checks, duplicate entries)
Date of Last Data Collection Procedure Review
Control Chart Selection & Implementation
Details the appropriate control chart type chosen and its proper implementation for the monitored process.
What type of control chart is being used?
If 'Other' was selected, please specify the control chart type used.
Number of subgroups analyzed for control limit calculation.
Date of initial control chart implementation.
Is the control chart being monitored manually or automatically?
Frequency of data collection (e.g., hourly, daily, weekly).
Brief description of the process variables being monitored.
Control Limit Calculation & Validation
Focuses on ensuring control limits are calculated correctly and periodically validated for accuracy.
Number of Data Points Used for Initial Control Limit Calculation
Method Used for Control Limit Calculation (e.g., Moving Range, X-bar and R Chart)
D3/D4 Factor Used (if applicable)
Distribution Assumption for Data (e.g., Normal, Unknown)
Date of Last Control Limit Recalculation
Frequency of Control Limit Recalculation (in days/weeks/months)
Justification for Recalculation Frequency
Process Stability Evaluation Method (e.g., MSA, Process Capability Index)
Out-of-Control Action & Response
Outlines procedures for identifying, investigating, and correcting out-of-control conditions.
Number of Points Exceeding Control Limits
Detailed Description of the Out-of-Control Condition
Potential Root Cause Category (e.g., Material, Equipment, Operator, Method)
Investigation Steps Taken to Determine Root Cause
Corrective Actions Implemented
Date Corrective Action Implemented
Verification of Corrective Action (How Effectiveness Was Confirmed)
Resolution Status
Signature of Person Verifying Resolution
Documentation & Training
Covers the documentation of SPM procedures and training provided to personnel involved.
Number of Personnel Trained on SPM Procedures
Date of Last SPM Training Session
Brief Summary of SPM Training Content
Copy of SPM Training Materials (e.g., manual, slides)
Type of Training Provided (Check all that apply)
Description of refresher training schedule
Are training records readily accessible?
Summary of the documentation procedures for SPM?
Periodic Review & Improvement
Addresses the ongoing review of SPM system effectiveness and opportunities for improvement.
Date of Last SPM System Review
Frequency of System Review (Months)
Summary of Review Findings
Action Items Identified During Review
Were any control charts deemed ineffective?
Areas for potential improvement?
Description of Actions Taken to Address Improvements
Target Completion Date for Improvement Actions
Name of Person Responsible for Improvement Actions
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