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SOP for Water System Maintenance

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SOP for Water System Maintenance

Standard Operating Procedure for Water System Maintenance

1) Purpose

The purpose of this SOP is to establish procedures for the maintenance of water systems used in the manufacturing of dental dosage forms to ensure water quality and compliance with regulatory standards.

2) Scope

This SOP applies to all water systems used for manufacturing processes involving dental pastes, gels, and mouthwashes within the pharmaceutical industry.

3) Responsibilities

The Facilities Management Department is responsible for conducting maintenance of the water system. The Quality Assurance (QA) Department is responsible for verifying compliance with this SOP.

See also  SOP for Handling and Storage of Finished Products

4) Procedure

4.1 Routine Maintenance

4.1.1 Develop a schedule for routine maintenance activities based on manufacturer’s recommendations and regulatory requirements.

4.1.2 Inspect water system components including filters, pipes, valves, and tanks for leaks, corrosion, or contamination.

4.1.3 Clean or replace filters and filter cartridges as per maintenance schedule.

4.2 Disinfection Procedures

4.2.1 Develop and follow procedures for periodic disinfection of the water system.

4.2.2 Use approved disinfectants and sanitizers at specified concentrations and contact times.

4.2.3 Flush and purge the water system after disinfection to remove residual disinfectants.

4.3 Calibration and Testing

4.3.1 Calibrate monitoring and control instruments such as pH meters and conductivity meters as per calibration schedule.

See also  SOP for Equipment Qualification Protocols

4.3.2 Perform water quality testing including microbial and chemical analysis according to established procedures.

4.4 Emergency Response

4.4.1 Respond promptly to water system failures, leaks, or contamination events.

4.4.2 Document emergency response activities and any corrective actions taken.

4.5 Record Keeping

4.5.1 Maintain records of all water system maintenance activities, including inspections, repairs, disinfections, and testing results.

4.5.2 Document any deviations from maintenance procedures and corrective actions taken.

4.6 Validation and Verification

4.6.1 Validate water system performance through periodic testing and validation activities.

4.6.2 Verify water quality parameters to ensure compliance with specified standards and requirements.

5) Abbreviations, if any

QA – Quality Assurance

See also  SOP for Environmental Impact Assessment of Equipment

pH – Potential of Hydrogen

6) Documents, if any

Water System Maintenance Log

Disinfection Records

Water Quality Test Reports

7) Reference, if any

Current Good Manufacturing Practices (cGMP) guidelines

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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