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SOP for Batch Reconciliation in Transdermal Patches Production

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SOP for Batch Reconciliation in Transdermal Patches Production

Standard Operating Procedure for Batch Reconciliation in Transdermal Patches Production

1) Purpose

The purpose of this SOP is to establish procedures for conducting batch reconciliation during the production of transdermal patches to ensure accuracy and completeness of manufacturing records.

2) Scope

This SOP applies to batch reconciliation activities performed after completion of each batch of transdermal patches within the production area.

3) Responsibilities

The Production Department is responsible for executing batch reconciliation as per this SOP. Quality Assurance (QA) personnel may oversee and verify reconciliation activities.

4) Procedure

4.1 Initial Preparation

  • 4.1.1 Collect all relevant batch records, production logs, and documentation pertaining to the completed batch of transdermal patches.
  • 4.1.2 Ensure batch records are accurate, complete, and signed off by responsible personnel at each stage of production.
See also  SOP for Use of Adhesives in Transdermal Patches Production

4.2 Components and Materials Reconciliation

  • 4.2.1 Verify reconciliation of raw materials and packaging components used against the quantities documented in batch records.
  • 4.2.2 Record any discrepancies found during reconciliation and investigate root causes as per established procedures.

4.3 In-Process and Finished Product Inventory

  • 4.3.1 Compare in-process inventory quantities (e.g., semi-finished patches) documented in batch records with physical counts.
  • 4.3.2 Conduct final reconciliation of finished product units manufactured against the expected output documented in batch records.

4.4 Documentation Review

  • 4.4.1 Review all batch records, reconciliation
reports, and related documentation for accuracy and completeness.
  • 4.4.2 Ensure that any deviations or discrepancies identified during reconciliation are documented and investigated according to deviation handling procedures.
  • 4.5 Approval and Release

    • 4.5.1 Obtain approval from authorized personnel for batch reconciliation and release of transdermal patches for further processing or packaging.
    • 4.5.2 Archive reconciled batch records and associated documentation in accordance with established record retention policies.

    5) Abbreviations, if any

    SOP: Standard Operating Procedure
    QA: Quality Assurance

    6) Documents, if any

    Batch Records
    Reconciliation Reports
    Deviation Investigation Reports

    7) Reference, if any

    ICH Q7: Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients
    ISO 13485: Medical devices – Quality management systems

    8) SOP Version

    Version 1.0

    See also  SOP for Customer Complaints Handling for Transdermal Patches
    Transdermal Patches Tags:Adhesion Testing Protocol, Analytical Method Development SOP, Assay of Active Ingredient SOP, Contamination Prevention SOP, Documentation SOP, Equipment calibration SOP, Equipment Cleaning SOP, Final Product Inspection SOP, Formulation development SOP, Homogeneity Testing SOP, In-process Testing SOP, Microbial Testing SOP, Personnel Training SOP, Process Optimization SOP, Process Validation SOP, Quality Control Transdermal Patches, Raw Material Inspection SOP, Release Rate Testing SOP, Sample Collection SOP, Sterility Maintenance SOP, Storage Conditions Transdermal Patches, Thickness Testing Procedure, Transdermal Patch Manufacturing SOP, Transdermal Patch Stability Testing, Waste Handling SOP

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    Standard Operating Procedures V 1.0

    • Aerosols
    • Analytical Method Development
    • Bioequivalence Bioavailability Study
    • Capsule Formulation
    • Clinical Studies
    • Creams
    • Data Integrity
    • Dental Dosage Forms
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    • Raw Material Stores
    • Regulatory Affairs
    • Tablet Manufacturing
    • Rectal Dosage Forms
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    • Validations and Qualifications

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    NEW! Revised SOPs – V 2.0

    • Aerosols V 2.0
    • Analytical Method Development V 2.0
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