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SOP for Jacketed Mixing Vessel

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SOP for Jacketed Mixing Vessel

Standard Operating Procedure for Jacketed Mixing Vessel

1) Purpose

The purpose of this SOP is to describe the procedure for the proper operation and maintenance of the Jacketed Mixing Vessel used in the pharmaceutical manufacturing of otic dosage forms to ensure efficient mixing and temperature control.

2) Scope

This SOP applies to all personnel involved in the operation and maintenance of the Jacketed Mixing Vessel in the pharmaceutical manufacturing facility.

3) Responsibilities

Operators: Responsible for correctly operating the Jacketed Mixing Vessel as per this SOP.
Quality Control (QC) Personnel: Responsible for monitoring the quality of mixing and temperature control.
Maintenance Personnel: Responsible for maintaining the Jacketed Mixing Vessel in proper working condition.

See also  SOP for Volumetric Filling Machine

4) Procedure

4.1 Pre-operation Checks
4.1.1 Inspection
4.1.1.1 Inspect the Jacketed Mixing Vessel for cleanliness and integrity before use.
4.1.1.2 Check jacket for leaks and ensure all connections are secure.
4.1.1.3 Verify that temperature control devices are functioning properly.

4.1.2 Preparation
4.1.2.1 Clean and sanitize the Jacketed Mixing Vessel and surrounding area.
4.1.2.2 Check and prepare all materials and ingredients required for mixing.
4.1.2.3 Ensure

that utilities (steam, cooling water, etc.) are connected and ready for operation.

4.2 Operation
4.2.1 Mixing Process
4.2.1.1 Power on the Jacketed Mixing Vessel and set temperature controls as per batch requirements.
4.2.1.2 Load materials into the vessel as per the formulation.
4.2.1.3 Initiate mixing process and monitor for uniformity and consistency.

See also  SOP for SIP (Sterilize-in-Place) System

4.2.2 Temperature Control
4.2.2.1 Monitor and adjust jacket temperature to maintain desired process temperature.
4.2.2.2 Record temperature readings and control settings at regular intervals.
4.2.2.3 Ensure that product temperature remains within specified limits throughout the mixing process.

4.3 Post-operation
4.3.1 Shutdown
4.3.1.1 Complete the mixing process and transfer mixture to designated containers or further processing steps.
4.3.1.2 Clean and sanitize the Jacketed Mixing Vessel and associated equipment thoroughly.
4.3.1.3 Perform post-operation checks to ensure no residual material in the vessel.

4.3.2 Maintenance
4.3.2.1 Inspect and clean mixing blades and vessel interior after each use.
4.3.2.2 Perform preventive maintenance on temperature control devices and jacket.
4.3.2.3 Document all maintenance activities and keep maintenance records updated.

See also  SOP for Magnetic Stirrer

5) Abbreviations, if any

QC: Quality Control
SOP: Standard Operating Procedure

6) Documents, if any

Maintenance records
Batch records for each mixing process
Calibration records for temperature control devices

7) Reference, if any

Manufacturer’s manual for the Jacketed Mixing Vessel
Pharmacopeial guidelines for pharmaceutical mixing processes

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

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