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SOP Guide for Pharma

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SOP for SOP for Contamination Control System Standard O…

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SOP for Contamination Control System

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

1) Purpose

The purpose of this SOP is to establish procedures for the operation and maintenance of the contamination control system to prevent contamination of ocular dosage forms during manufacturing.

2) Scope

This SOP applies to all contamination control measures and systems within the facility that are designed to maintain cleanliness and prevent contamination during the manufacturing process of ocular dosage forms.

3) Responsibilities

Facility management and quality assurance personnel are responsible for ensuring compliance with this SOP. Operations personnel are responsible for following procedures outlined in this SOP.

See also  SOP for SOP for Environmental MonitoringStandard Opera...

4) Procedure

4.1 Monitoring and Control

  1. Regularly monitor environmental conditions using calibrated instruments.
  2. Implement measures to control contamination sources in manufacturing areas.
  3. Monitor and maintain cleanliness of production equipment and facilities.

4.2 Cleaning and Disinfection

  1. Develop and follow cleaning and disinfection procedures for manufacturing areas and equipment.
  2. Use approved cleaning agents and methods according to validated procedures.
  3. Ensure thorough cleaning of critical surfaces and equipment between batches.

4.3 Personnel Hygiene

  1. Enforce strict personnel hygiene practices, including gowning and hand hygiene protocols.
  2. Provide regular training to personnel on contamination control measures and practices.

4.4 Material and Equipment Handling

  1. Ensure proper handling and storage of raw materials and components to prevent contamination.
  2. Validate cleaning procedures for equipment used
in manufacturing processes.

4.5 Monitoring and Documentation

  1. Maintain records of environmental monitoring results and contamination control activities.
  2. Document any deviations from established procedures and corrective actions taken.

5) Abbreviations, if any

SOP: Standard Operating Procedure

6) Documents, if any

  1. Contamination control plan
  2. Cleaning validation reports
  3. Environmental monitoring records

7) Reference, if any

GMP Guidelines for Pharmaceutical Manufacturing

8) SOP Version

Version 1.0

See also  SOP for Sterile Filtration
Ocular (Eye) Dosage Forms Tags:Aseptic processing, Bioavailability in ocular drugs, Blow-fill-seal technology, Cleanroom standards, Conjunctival inserts, Contact lenses drug delivery, Drug stability testing, Ethylene oxide sterilization, Eye drops SOP, Gamma sterilization, Heat sterilization, HEPA filtration, Intraocular implants, Intraocular injections, Microemulsions in ophthalmics, Mucoadhesive polymers, Multidose ophthalmic bottles, ocular dosage forms, Ocular drug delivery, Ointment preparation, Ophthalmic formulations, Ophthalmic gels, Ophthalmic suspensions, Ophthalmic viscosity, Preservative-free formulations, Solubility issues, SOP for Ocular Dosage Forms, Sterile filtration, Sterile solutions, Sterility testing, Terminal sterilization, Topical ocular drugs

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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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