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SOP for Process Control System

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SOP for Process Control System

SOP for Process Control System

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

1) Purpose

The purpose of this SOP is to establish procedures for the control and monitoring of manufacturing processes in the production of ocular dosage forms to ensure product quality and consistency.

2) Scope

This SOP applies to all process control systems and measures implemented within the facility to regulate and monitor critical manufacturing processes for ocular dosage forms.

See also  SOP for Packaging Machine for Eye Drops

3) Responsibilities

Quality assurance personnel are responsible for overseeing the implementation and compliance of this SOP. Production personnel are responsible for adhering to procedures outlined in this document.

4) Procedure

4.1 Process Monitoring and Control

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    SOP for Process Control System

    Standard Operating

Procedure for Process Control System in Ocular Dosage Form Manufacturing

1) Purpose

The purpose of this SOP is to establish procedures for the control and monitoring of manufacturing processes in the production of ocular dosage forms to ensure product quality and consistency.

2) Scope

This SOP applies to all process control systems and measures implemented within the facility to regulate and monitor critical manufacturing processes for ocular dosage forms.

3) Responsibilities

Quality assurance personnel are responsible for overseeing the implementation and compliance of this SOP. Production personnel are responsible for adhering to procedures outlined in this document.

4) Procedure

4.1 Process Monitoring and Control

  1. Set up and calibrate process control instruments according to manufacturer’s specifications.
  2. Monitor critical process parameters such as temperature, pressure, flow rates, and pH continuously during manufacturing.
  3. Implement control measures to ensure process parameters remain within specified limits.

4.2 Process Validation

  1. Validate manufacturing processes according to approved protocols and regulatory guidelines.
  2. Document and review process validation results to ensure compliance with predetermined criteria.

4.3 Process Adjustments and Corrective Actions

  1. Authorize adjustments to process parameters based on validated procedures and documented changes.
  2. Implement corrective actions promptly in response to deviations or non-conformances identified during process monitoring.

4.4 Process Documentation

  1. Maintain accurate records of process parameters, adjustments, and monitoring activities.
  2. Document changes to manufacturing processes and obtain necessary approvals before implementation.

5) Abbreviations, if any

SOP: Standard Operating Procedure

6) Documents, if any

  1. Process validation protocols and reports
  2. Process control instrument calibration records
  3. Process monitoring logs

7) Reference, if any

GMP Guidelines for Pharmaceutical Manufacturing

8) SOP Version

Version 1.0

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

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