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Elixir Department: SOP for Vortex Mixer Operation for Lab Batches – V 2.0

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Elixir Department: SOP for Vortex Mixer Operation for Lab Batches – V 2.0

Standard Operating Procedure for Vortex Mixer Operation for Lab Batches in Elixir Manufacturing

Department Elixir Department
SOP No. SOP/ELX/138/2025
Supersedes SOP/ELX/138/2022
Page No. Page 1 of 10
Issue Date 11/04/2025
Effective Date 15/04/2025
Review Date 11/04/2026

1. Purpose

To outline the standard procedure for the operation and maintenance of vortex mixers used during small-scale/laboratory batch preparations in the Elixir Department. This ensures consistent mixing of elixir samples and homogeneity of test formulations.

2. Scope

This SOP applies to all laboratory vortex mixers used for pre-formulation studies, analytical sample preparation, or small lab-scale elixir batches in the R&D or QC sections of the Elixir Department.

3. Responsibilities

  • QC/R&D Analyst:
    • Operate the vortex mixer according to this SOP.
    • Ensure the equipment is clean and functioning prior to use.
  • Supervisor:
    • Ensure training of personnel and review of logbooks.
  • Engineering:
    • Handle any equipment repairs or calibration issues.
  • QA:
    • Verify usage logs and cleanliness status before use.
See also  Elixir Department: SOP for In-process Sampling During Elixir Manufacturing - V 2.0

4. Accountability

The QC/R&D Head is accountable for ensuring correct usage and documentation of vortex mixer operations. The Engineering Head is accountable for maintenance and calibration.

5. Procedure

5.1 Pre-Use Checks

  1. Ensure the vortex mixer is labeled “CLEANED” and has a valid calibration sticker (if applicable).
  2. Check that the power cord and plug are undamaged and properly connected to the power source.
  3. Ensure the platform or cup head is securely fitted and free from visible contamination.

5.2 Operating the Vortex Mixer

  1. Place the tube or container to be mixed on the center of the vortex platform or press gently onto the cup head.
  2. Set the mixing speed (RPM) and time using the control dial or digital panel as required by the procedure.
  3. Select “touch” mode for intermittent mixing or “continuous” mode for hands-free operation.
  4. Start the mixer and monitor the motion. Ensure the sample is properly secured and is not splashing or leaking.
  5. After mixing is complete, remove the tube carefully and wipe the platform if any spillage occurred.
See also  Elixir Department: SOP for Cleaning of Inline Filters and Screens - V 2.0

5.3 Post-Use Cleaning

  1. Switch off the equipment and unplug it from the power source.
  2. Wipe the platform, head, and housing with a lint-free cloth moistened with 70% IPA.
  3. Label the equipment as “CLEANED” and record usage in the Equipment Logbook (Annexure-1).

5.4 Precautions

  1. Do not use damaged or cracked glassware with the vortex mixer.
  2. Do not apply excessive pressure to the cup head to avoid motor damage.
  3. Ensure the surface under the mixer is flat and vibration-resistant.
  4. Do not operate the mixer with wet hands or near water sources.

6. Abbreviations

  • SOP: Standard Operating Procedure
  • R&D: Research and Development
  • QA: Quality Assurance
  • IPA: Isopropyl Alcohol
See also  Elixir Department: SOP for Air Drying Process of Cleaned Components - V 2.0

7. Documents

  1. Equipment Usage Log (Annexure-1)
  2. Cleaning Log (if maintained separately)

8. References

  • 21 CFR Part 211 – Current Good Manufacturing Practice
  • WHO TRS 1010 – Laboratory Practices
  • Manufacturer’s Operating Manual

9. SOP Version

Version: 2.0

10. Approval Section

Prepared By Checked By Approved By
Signature
Date
Name
Designation
Department

11. Annexures

Annexure-1: Equipment Usage Log

Date Sample ID Batch No. Mixing Time (s) Speed (RPM) Mode Used Operator Remarks
11/04/2025 PRE-ELX-003 DEV-ELX-12 60 2000 Touch Sunita Reddy Uniform Mixing Achieved

Revision History:

Revision Date Revision No. Revision Details Reason for Revision Approved By
01/01/2024 1.0 Initial SOP Release New SOP QA Head
11/04/2025 2.0 Updated log table and cleaning steps Process Enhancement QA Head
Elixers V 2.0 Tags:Elixir colorants, Elixir dosage form, Elixir filtration techniques, Elixir flavoring agents, Elixir formulation, Elixir GMP compliance, Elixir manufacturing process, Elixir manufacturing SOPs, Elixir packaging requirements, Elixir pharmacopoeial standards, Elixir preparation methods, Elixir preservatives, Elixir production equipment, Elixir quality control, Elixir regulatory guidelines, Elixir shelf life, Elixir stability testing, Elixir sterilization methods, Elixir storage conditions, Elixir sweetening agents, Elixir viscosity modifiers, Hydroalcoholic solutions, Medicated elixirs, Non-medicated elixirs, Pharmaceutical elixirs

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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
  • Gels V 2.0
  • Injectables 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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