PHARMACEUTICAL VALIDATION CHECKLIST TEMPLATE Created by ChecklistGuro (https://checklistguro.com) --- PLANNING & SCOPE DEFINITION --- [ ] Project Objective [ ] Scope Description (Inclusions & Exclusions) [ ] Validation Type (e.g., Prospective, Concurrent, Retrospective) (Prospective, Concurrent, Retrospective) [ ] Project Start Date [ ] Estimated Completion Time (in days) [ ] Critical Process Parameters (Initial Assessment) --- RISK ASSESSMENT --- [ ] Process/Equipment Description [ ] Potential Hazards/Failure Modes [ ] Likelihood of Occurrence (1-5) [ ] Severity of Impact (1-5) [ ] Risk Score (Likelihood x Severity) [ ] Risk Level (Low, Medium, High) (Low, Medium, High) [ ] Control Measures/Mitigation Strategies [ ] Effectiveness of Control Measures (Adequate/Inadequate) (Adequate, Inadequate) --- DESIGN & SPECIFICATION REVIEW --- [ ] Describe the intended function of the equipment/process. [ ] Upload design drawings or schematics. [ ] Specify critical operating parameters (e.g., temperature, pressure). [ ] Does the design meet relevant regulatory requirements (e.g., GMP, FDA)? (Yes, No, Not Applicable) [ ] Explain any deviations from standard designs and justification for these deviations. [ ] Date of Design Specification Review [ ] Reviewer Signature --- INSTALLATION QUALIFICATION (IQ) --- [ ] Equipment Name [ ] Manufacturer [ ] Serial Number [ ] Installation Date [ ] Detailed Description of Equipment and Location [ ] Utilities Connected (Select All That Apply) (Electricity, Water, Compressed Air, Nitrogen, HVAC) [ ] Installation Vendor [ ] Installation Technician Signature --- OPERATIONAL QUALIFICATION (OQ) --- [ ] Operating Temperature (Minimum) [ ] Operating Temperature (Maximum) [ ] Pressure (Minimum) [ ] Pressure (Maximum) [ ] Date of First OQ Run [ ] Start Time of First OQ Run [ ] Equipment Status After OQ (Operational, Requires Calibration, Requires Repair) [ ] Observations During OQ Runs [ ] OQ Execution Signature --- PERFORMANCE QUALIFICATION (PQ) --- [ ] Batch Number(s) Tested [ ] Start Date of PQ Runs [ ] End Date of PQ Runs [ ] Number of PQ Batches/Runs Completed [ ] Summary of PQ Results and Observations [ ] PQ Criteria Met? (Yes, No, N/A) [ ] Attachment: PQ Data Reports/Charts [ ] Signature of PQ Reviewer --- DOCUMENTATION & RECORDS --- [ ] Validation Protocol Reference Number [ ] Validation Protocol Document [ ] Protocol Creation Date [ ] Protocol Review Date [ ] Protocol Reviewer Signature [ ] Summary of Findings/Deviations [ ] Report Approval Signature [ ] Number of Pages in Report --- CHANGE CONTROL --- [ ] Date of Change Request [ ] Description of Change [ ] Justification for Change [ ] Impact Assessment (High/Medium/Low) (High, Medium, Low) [ ] Estimated Implementation Time (Days) [ ] Affected Systems/Equipment (Equipment A, Software B, Process C, Documentation D) [ ] Requestor Signature [ ] Approval Date [ ] Approval Signature --- REVIEW & APPROVAL --- [ ] Review Date [ ] Reviewer Name [ ] Review Comments [ ] Approval Status (Approved, Rejected, Conditional Approval) [ ] Approval Reason (if rejected/conditional) [ ] Approver Signature [ ] Approval Date --- END OF TEMPLATE --- Transform this text into a digital, automated, and trackable mobile app! Visit: https://checklistguro.com/templates/pharmaceutical/pharmaceutical-validation-checklist-template (Click "Install Template" to launch your digital inspection tool immediately)