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SOP for Temperature Control System

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SOP for Temperature Control System

Standard Operating Procedure for Temperature Control System in Ocular Dosage Form Manufacturing

1) Purpose

The purpose of this SOP is to establish procedures for the operation, monitoring, and maintenance of the temperature control system used in the manufacturing of ocular dosage forms to ensure consistent temperature conditions that meet regulatory standards.

2) Scope

This SOP applies to all temperature control systems within the facility used for maintaining controlled temperature conditions in the manufacturing areas for ocular dosage forms.

3) Responsibilities

Facility management and maintenance personnel are responsible for the operation, monitoring, and maintenance of the temperature control system. Quality assurance personnel are responsible for overseeing compliance with regulatory requirements and standards.

See also  SOP for Syringe Sealing System

4) Procedure

4.1 Start-up and Shutdown Procedures

  1. Ensure all personnel are trained on start-up and shutdown procedures for the temperature control system.
  2. Check and verify power supply to the temperature control unit before starting.
  3. Follow manufacturer’s instructions for starting up and shutting down the system.

4.2 Routine Operation

  1. Monitor and record temperature regularly using calibrated instruments.
  2. Adjust operational settings as necessary to maintain specified temperature conditions.
  3. Monitor alarm systems and respond promptly to any deviations or abnormalities.

4.3 Maintenance and Calibration

  1. Schedule routine maintenance activities based on manufacturer’s recommendations and facility-specific requirements.
  2. Verify the accuracy of temperature control instruments through regular calibration.
  3. Replace or
repair any malfunctioning components to ensure optimal performance.

4.4 Cleaning and Sanitization

  1. Clean external surfaces of the temperature control unit regularly using approved cleaning agents and methods.
  2. Sanitize internal components of the temperature control unit as per validated procedures to prevent contamination.

4.5 Emergency Procedures

  1. Develop and maintain emergency procedures for power failures, equipment malfunctions, or other emergencies affecting the temperature control system.
  2. Train personnel on emergency response procedures and ensure the availability of backup systems or contingency plans.

4.6 Documentation and Records

  1. Maintain records of routine operations, maintenance activities, and calibration results.
  2. Document any deviations from standard procedures and corrective actions taken.

4.7 Training

  1. Provide training to personnel involved in the operation, maintenance, and monitoring of the temperature control system.
  2. Ensure personnel are aware of SOP updates and revisions related to the temperature control system.

5) Abbreviations, if any

SOP: Standard Operating Procedure

6) Documents, if any

  1. Temperature control system maintenance log
  2. Calibration certificates
  3. Emergency response plan

7) Reference, if any

GMP Guidelines for Pharmaceutical Manufacturing

8) SOP Version

Version 1.0

See also  SOP for Packaging Line for Eye Drops
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Next Post: SOP for Lyophilizer

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

  • Aerosols V 2.0
  • Analytical Method Development V 2.0
  • API Manufacturing V 2.0
  • BA-BE Studies V 2.0
  • Biosimilars V 2.0
  • Capsules V 2.0
  • Creams V 2.0
  • Elixers V 2.0
  • Ointments V 2.0
  • Raw Material Warehouse V 2.0
  • Tablet Manufacturing V2.0

New Publication: A must for All.

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