PHARMACEUTICAL PROCESS VALIDATION CHECKLIST TEMPLATE

Created by ChecklistGuro (https://checklistguro.com)

--- PROTOCOL DEVELOPMENT ---
[ ] Protocol Objective(s)
[ ] Batch Size (Proposed)
[ ] Validation Type (e.g., Prospective, Concurrent, Retrospective) (Prospective, Concurrent, Retrospective)
[ ] Protocol Start Date (Planned)
[ ] Critical Process Parameters (CPPs) (Temperature, Pressure, pH, Mixing Speed, Humidity, Time)
[ ] Initial Process Flow Diagram

--- PROCESS UNDERSTANDING & RISK ASSESSMENT ---
[ ] Detailed Process Description
[ ] Critical Process Parameter (CPP) - Upper Limit
[ ] Critical Process Parameter (CPP) - Lower Limit
[ ] Potential Failure Mode (Equipment Malfunction, Material Variation, Operator Error, Environmental Factors)
[ ] Risk Mitigation Strategy
[ ] Risk Score (Severity x Probability)
[ ] Factors Influencing Risk (Raw Material Quality, Equipment Calibration, Operator Training, Environment Control)

--- EQUIPMENT QUALIFICATION ---
[ ] Equipment Serial Number
[ ] Installation Date
[ ] Equipment Description & Specifications
[ ] Qualification Phase (IQ, OQ, PQ) (Installation Qualification (IQ), Operational Qualification (OQ), Performance Qualification (PQ))
[ ] Temperature Setpoint (Â°C)
[ ] Temperature Recorded (Â°C)
[ ] Duration of Stability Test (hours)
[ ] Qualified By

--- MATERIAL QUALIFICATION ---
[ ] Material Name
[ ] Lot Number
[ ] Receipt Date
[ ] Supplier (Supplier A, Supplier B, Supplier C)
[ ] Purity (%)
[ ] Supplier CoA Review Comments
[ ] CoA Document
[ ] Material Status (Approved, Pending Review, Rejected)

--- PROCESS PARAMETER MONITORING ---
[ ] Temperature (Run 1)
[ ] Temperature (Run 1) - Min
[ ] Temperature (Run 1) - Max
[ ] Pressure (Run 1)
[ ] Humidity (Run 1)
[ ] Date of Reading (Run 1)
[ ] Time of Reading (Run 1)
[ ] Reading Status (Run 1) (Within Specification, Out of Specification, Unverified)

--- SAMPLING & TESTING ---
[ ] Sample Size (n)
[ ] Sampling Method (Random Sampling, Stratified Sampling, Systematic Sampling)
[ ] Sampling Date
[ ] Sampling Time
[ ] Test Method (e.g., USP) (USP <1>, USP <2>, In-house Method)
[ ] Result 1 (Numeric)
[ ] Result 2 (Numeric)
[ ] Test Comments/Observations

--- DATA ANALYSIS & EVALUATION ---
[ ] Batch Size
[ ] Number of Validation Batches
[ ] Acceptance Criteria Threshold (e.g., % Deviation)
[ ] Statistical Method Used (e.g., ANOVA, t-test) (ANOVA, t-test, Regression Analysis, Other)
[ ] Summary of Statistical Analysis Results
[ ] Process Capability (Cp/Cpk) (Cp >= 1.33, Cpk >= 1.33, Other)
[ ] Justification for Acceptance/Rejection of Batch

--- DEVIATION MANAGEMENT ---
[ ] Deviation Description
[ ] Date of Deviation
[ ] Time of Deviation
[ ] Deviation Severity (e.g., Minor, Major, Critical) (Minor, Major, Critical)
[ ] Batch Number Affected (if applicable)
[ ] Affected Area(s) (e.g., Manufacturing, QC, Packaging) (Manufacturing, QC, Packaging, Warehouse, Other)
[ ] Root Cause Analysis
[ ] Corrective Action Plan
[ ] Corrective Action Completion Date

--- REPORTING & DOCUMENTATION ---
[ ] Executive Summary of Validation Results
[ ] Complete Validation Protocol Document
[ ] Number of Validation Batches Executed
[ ] Summary of Deviations and Corrective Actions
[ ] Report Completion Date
[ ] Validation Manager Signature
[ ] Detailed Statistical Analysis Results

--- CHANGE CONTROL & CONTINUOUS IMPROVEMENT ---
[ ] Date of Change Request
[ ] Description of Change Request
[ ] Change Category (e.g., Equipment, Process, Material) (Equipment, Process, Material, Personnel, Other)
[ ] Estimated Impact Score (1-5, 5 being highest impact)
[ ] Affected Areas/Departments (Manufacturing, Quality Assurance, Engineering, Validation, Supply Chain)
[ ] Change Control Number
[ ] Implementation Date

--- END OF TEMPLATE ---
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