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Sterile Injectable Manufacturing: SOP for Automation System Checks in Injectable Filling Lines – V 2.0

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Sterile Injectable Manufacturing: SOP for Automation System Checks in Injectable Filling Lines – V 2.0

Standard Operating Procedure for Automation System Checks in Injectable Filling Lines


Department Sterile Injectable Manufacturing
SOP No. SOP/SIM/148/2025
Supersedes SOP/SIM/148/2022
Page No. Page 1 of 15
Issue Date 24/06/2025
Effective Date 26/06/2025
Review Date 24/06/2026

1. Purpose

This SOP describes the procedure for performing checks, verifications, and validations of automation systems installed in sterile injectable filling lines to ensure they function reliably, accurately, and in compliance with Good Manufacturing Practices

(GMP).

2. Scope

This SOP is applicable to all automated components of the filling lines including programmable logic controllers (PLCs), human-machine interfaces (HMIs), servo systems, SCADA interfaces, and associated software control systems in the sterile injectable production area.

3. Responsibilities

  • Automation Engineer: Conduct scheduled checks and validations, maintain system backup and logs.
  • Production Supervisor: Verify automation performance during operations and report abnormalities.
  • QA Officer: Review compliance records, deviations, and validate system changes.

4. Accountability

The Head of Engineering is accountable for ensuring this SOP is followed, and QA Head is accountable for GMP oversight and final approval of any changes to automation systems.

See also  Sterile Injectable Manufacturing: SOP for Designing Stability-Indicating Formulations - V 2.0

5. Procedure

5.1 System Overview and Components

  • PLC: Controls logic and operations of filling, stoppering, and movement mechanisms.
  • HMI: Operator interface for parameter display and command input.
  • Servo Drives: Control motion precision for filling accuracy.
  • SCADA: Supervisory system for centralized monitoring, alarms, and reporting.

5.2 Daily Checks before Batch Start

  1. Power ON sequence should follow system design (PLC → HMI → SCADA).
  2. Verify touchscreen calibration and responsiveness of HMI.
  3. Check for absence of unresolved alarms or error codes.
  4. Ensure communication status between PLC and peripherals is green (Annexure-1).
  5. Verify interlocks such as vial presence detection, fill-no-vial logic, safety door lock, etc.

5.3 System Validation and Backup

  1. All new installations must undergo IQ, OQ, and PQ before operational use.
  2. Version control must be maintained for all PLC logic, HMI scripts, and SCADA programs.
  3. System backups must be stored offline and updated monthly.

5.4 Periodic Preventive Maintenance Checks

  1. Verify software patch updates if applicable (Annexure-2).
  2. Test emergency shutdown systems and alarm activation monthly.
  3. Perform system cleaning using ESD-safe tools; avoid chemical contact with HMIs.
See also  Sterile Injectable Manufacturing: SOP for Review of Batch Manufacturing Records - V 2.0

5.5 Alarm & Event Management

  1. Ensure that all critical alarms (e.g., fill error, servo fault, vial jam) are active and loggable.
  2. Alarms must be time-stamped and reviewed by Production and QA at batch end.
  3. Deviations must be logged when alarms impact process integrity (Annexure-3).

5.6 User Access Control and Audit Trails

  1. User roles must be defined (Operator, Supervisor, Admin).
  2. Passwords must expire every 90 days and be changed immediately upon personnel departure.
  3. Audit trails must be enabled and non-editable. QA must review trails for every batch (Annexure-4).

5.7 Documentation and Reporting

  1. Maintain Automation System Check Log for each day the system is used (Annexure-5).
  2. Backup schedules and logs must be reviewed monthly by the Engineering Head.
  3. Deviations, changes, or errors must be recorded in Change Control System.

6. Abbreviations

  • SOP: Standard Operating Procedure
  • PLC: Programmable Logic Controller
  • HMI: Human Machine Interface
  • GMP: Good Manufacturing Practice
  • SCADA: Supervisory Control and Data Acquisition

7. Documents

  • Annexure-1: Daily Automation System Pre-Check Sheet
  • Annexure-2: Preventive Maintenance Log
  • Annexure-3: Alarm Deviation Report
  • Annexure-4: Audit Trail Review Template
  • Annexure-5: Automation System Check Log
See also  Sterile Injectable Manufacturing: SOP for Formulation Development of Subcutaneous Injections - V 2.0

8. References

  • 21 CFR Part 11 – Electronic Records and Signatures
  • GAMP 5 – Good Automated Manufacturing Practice
  • ICH Q9 – Quality Risk Management

9. SOP Version

Version: 2.0

10. Approval Section

Prepared By Checked By Approved By
Signature
Date
Name
Designation Automation Engineer QA Executive Head QA
Department Engineering Quality Assurance Quality Assurance

11. Annexures

Annexure-1: Daily Automation System Pre-Check Sheet

Date System Check Item Status Operator
24/06/2025 Filling PLC Comms OK ✓ Ravi Kumar

Annexure-2: Preventive Maintenance Log

Date Component Activity Performed By
20/06/2025 SCADA Server Software Backup Ajay Verma

Annexure-3: Alarm Deviation Report

Alarm Date Cause Impact CAPA
Fill Volume Fault 22/06/2025 Nozzle Block Batch Hold Routine Filter Check

Annexure-4: Audit Trail Review Template

Date User Action System Module Reviewed By Comments
24/06/2025 Speed Change Servo Control QA Officer Acceptable

Annexure-5: Automation System Check Log

Date System Status Remarks Engineer
24/06/2025 PLC + HMI OK All Good Sachin Yadav

Revision History

Revision Date Version Description Reason Approved By
01/01/2022 1.0 Initial Issue New SOP QA Head
24/06/2025 2.0 Added Annexures and Updated Version Control Annual Review QA Head
Injectables V 2.0 Tags:Aseptic processing SOP, Aseptic technique in sterile manufacturing, Cleanroom SOP for injectables, SOP for ampoule sealing, SOP for autoclave sterilization, SOP for container closure integrity testing, SOP for environmental monitoring in aseptic area, SOP for gowning in cleanroom, SOP for in-process checks in sterile manufacturing, SOP for injectable formulation, SOP for lyophilizer operation, SOP for sterile filtration, SOP for sterilization validation, SOP for vial filling, SOP for visual inspection of injectables, Sterile area cleaning SOP, Sterile filling line SOP, Sterile injectable quality control SOP, Sterile injection SOP, Sterile manufacturing procedure

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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
  • Drug Discovery
  • Environment, Health and Safety
  • Formulation Development
  • Gels
  • Good Distribution Practice
  • Good Warehousing Practices
  • In-Process Control
  • Injectables
  • Liquid Orals
  • Liposome and Emulsion Formulations
  • Lotions
  • Lyophilized Products
  • Maintenance Dept.
  • Medical Devices
  • Metered-Dose Inhaler
  • Microbiology Testing
  • Nanoparticle Formulation
  • Nasal Spray Formulations
  • Nebulizers
  • Ocular (Eye) Dosage Forms
  • Ointments
  • Otic (Ear) Dosage Forms
  • Pharmacovigilance
  • Powder & Granules
  • Purchase Departments
  • Quality Assurance
  • Quality Control
  • Raw Material Stores
  • Regulatory Affairs
  • Tablet Manufacturing
  • Rectal Dosage Forms
  • Transdermal Patches
  • Vaginal Dosage Forms
  • Validations and Qualifications

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NEW! Revised SOPs – V 2.0

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