Preparation of Annual Product Review (APR)

📘 Preparation of Annual Product Review (APR)
The Annual Product Review (APR) (also referred to as Product Quality Review – PQR in EU) is a regulatory requirement under 21 CFR 211.180(e) and ICH Q7/Q10. Its purpose is to ensure product quality, process consistency, and regulatory compliance throughout the lifecycle.
🔹 Steps in Preparing APR
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Planning & Responsibility
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Establish an APR schedule for each product.
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Define responsibilities: QA usually coordinates, while QC, Production, Regulatory, and Supply Chain provide inputs.
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Data Collection
Gather data from the previous review period (usually 12 months):-
Batch records: number of batches manufactured, released, rejected.
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Deviations & CAPAs related to the product.
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OOS / OOT results in QC testing.
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Change controls implemented (formulation, process, equipment, supplier changes).
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Stability data (ongoing and commitment studies).
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Market complaints, returns, and recalls.
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Supplier qualification & raw material issues.
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Process validation & cleaning validation status.
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Equipment maintenance and calibration records.
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Trend Analysis
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Perform statistical evaluation of batch yield, critical process parameters (CPPs), and critical quality attributes (CQAs).
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Identify recurring deviations or quality signals.
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Assess compliance with specifications and acceptance criteria.
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Evaluation
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Determine if the product remains in a state of control.
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Evaluate need for re-validation or process improvements.
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Review adequacy of corrective and preventive actions.
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Assess effectiveness of change controls.
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Recommendations & Action Plan
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Summarize findings.
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Propose CAPA, process optimization, or additional training if needed.
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Document rationale for no further action if applicable.
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Approval & Archiving
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QA prepares the final APR report.
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Get approvals from Quality Head and site management.
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Ensure timely archival and readiness for inspection.
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✅ Benefits of APR
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Ensures product and process consistency.
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Helps detect trends before they lead to failures.
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Demonstrates compliance during regulatory inspections.
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Supports continual improvement.
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