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SOP for Water System Maintenance in Creams Production

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SOP for Water System Maintenance in Creams Production

Standard Operating Procedure for Water System Maintenance in Creams Production

1) Purpose

The purpose of this SOP is to establish guidelines and procedures for the maintenance of the water system used in creams production to ensure a continuous supply of high-quality water that meets all regulatory standards and maintains product quality and safety.

2) Scope

This SOP applies to all components of the water system used in creams production, including water purification, storage, and distribution systems.

3) Responsibilities

The Engineering and Maintenance department is responsible for the implementation and execution of water system maintenance. The Quality Assurance (QA) department is responsible for monitoring and verifying the effectiveness of the maintenance activities.

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4) Procedure

4.1 Preventive Maintenance Schedule

4.1.1 Develop a preventive maintenance schedule for all components of the water system, including filters, pumps, tanks, piping, and monitoring equipment.

4.1.2 Ensure the maintenance schedule is approved by the Engineering and QA departments.

4.1.3 Display the maintenance schedule in the engineering control room and update it regularly.

4.2 Routine Maintenance Activities

4.2.1 Replace or clean water filters at regular intervals as specified in the maintenance schedule.

4.2.2 Inspect and clean water storage tanks to prevent biofilm formation and contamination.

4.2.3 Check and maintain pumps and valves to ensure proper operation

and prevent leaks.

4.2.4 Inspect piping for leaks, corrosion, or blockages and repair or clean as necessary.

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4.2.5 Calibrate and test monitoring equipment, including sensors for pH, conductivity, and microbial contamination, to ensure accurate water quality monitoring.

4.3 Water Quality Monitoring

4.3.1 Perform regular water quality tests, including microbial testing, chemical analysis, and physical parameters (e.g., pH, conductivity) to ensure compliance with specified limits.

4.3.2 Maintain records of all water quality tests and review results to identify trends and areas for improvement.

4.3.3 Investigate any deviations from acceptable water quality standards and implement corrective actions promptly.

4.4 Corrective Maintenance

4.4.1 Address any water system malfunctions or deviations from specified performance parameters immediately.

4.4.2 Investigate the root cause of water system issues and implement corrective actions to prevent recurrence.

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4.4.3 Document all corrective maintenance activities, including root cause analysis and corrective actions taken.

4.5 Training and Compliance

4.5.1 Provide training for maintenance personnel on water system operation, maintenance procedures, and safety protocols.

4.5.2 Conduct periodic refresher training and competency assessments for maintenance personnel.

4.5.3 Ensure compliance with all relevant regulatory requirements and industry standards for water system maintenance in pharmaceutical production.

5) Abbreviations, if any

QA: Quality Assurance

6) Documents, if any

Preventive Maintenance Schedule

Maintenance Activity Records

Water Quality Test Records

Training Records

7) Reference, if any

US FDA CFR (Code of Federal Regulations) Part 211: Current Good Manufacturing Practice for Finished Pharmaceuticals

USP <1231>: Water for Pharmaceutical Purposes

8) SOP Version

Version 1.0

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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

  • 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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