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API Manufacturing: SOP for Solvent Transfer Using Pumps – V 2.0

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API Manufacturing: SOP for Solvent Transfer Using Pumps – V 2.0

Standard Operating Procedure for Solvent Transfer Using Pumps in API Manufacturing

Department API Manufacturing
SOP No. SOP/API/056/2025
Supersedes SOP/API/056/2022
Page No. Page 1 of 10
Issue Date 13/04/2025
Effective Date 15/04/2025
Review Date 13/04/2026

1. Purpose

To define the procedure for the safe and controlled transfer of solvents using pumps in API manufacturing, ensuring prevention of spills, cross-contamination, and exposure while maintaining GMP and safety compliance.

2. Scope

This SOP is applicable to all solvent transfers using mechanical, diaphragm, peristaltic, or centrifugal pumps within the API manufacturing facility, including between drums, tanks, reactors, and pipelines.

3. Responsibilities

  • Operators: Ensure correct setup, operation, and cleaning of pumps used for solvent transfer.
  • Maintenance Team: Maintain pumps in working condition and respond to breakdowns.
  • EHS Team: Ensure transfer complies with safety standards and spill containment procedures.
  • QA Team: Review logs and verify GMP compliance.
See also  API Manufacturing: SOP for Intermediate Moisture Check using IR Balance - V 2.0

4. Accountability

The Production Head is accountable for ensuring all solvent transfers via pumps are carried out as per this SOP. The EHS Head is accountable for safety compliance.

5. Procedure

5.1 Pre-Transfer Checklist

  1. Verify the pump type is compatible with the solvent (e.g., explosion-proof for flammable solvents).
  2. Ensure grounding and bonding cables are connected to prevent static discharge.
  3. Check the availability of:
    • Appropriate PPE (gloves, goggles, antistatic shoes, face shield)
    • Spill kits and fire extinguishers nearby
    • Solvent transfer logbook

5.2 Solvent Transfer Process

  1. Connect inlet hose from solvent container (drum or tank) to the pump suction port securely.
  2. Connect discharge hose to receiving vessel, ensuring tight clamps and leak-free joints.
  3. Prime the pump if required (refer equipment manual).
  4. Switch on the pump and begin transfer slowly.
  5. Monitor solvent level and flow rate throughout the transfer.
  6. Do not leave the pump unattended during operation.
  7. Upon completion:
    • Switch off the pump
    • Drain remaining solvent in hoses to avoid wastage
    • Disconnect and clean hoses
See also  API Manufacturing: SOP for Review of Product Labels and Packaging Materials - V 2.0

5.3 Post-Transfer Activities

  1. Document transfer details in the “Solvent Transfer Log” (Annexure-1).
  2. Check for any leakage, spills, or abnormalities and report immediately.
  3. If cross-contamination risk exists, clean pump as per cleaning SOP before reuse.

5.4 Emergency Handling

  1. In case of leakage/spill:
    • Stop the pump immediately
    • Use spill kit to contain and clean
    • Ventilate the area
    • Report incident to shift in-charge and EHS
  2. Record all such incidents in “Solvent Spill and Incident Log” (Annexure-2).

6. Abbreviations

  • SOP: Standard Operating Procedure
  • PPE: Personal Protective Equipment
  • EHS: Environment, Health and Safety
  • QA: Quality Assurance

7. Documents

  1. Solvent Transfer Log (Annexure-1)
  2. Solvent Spill and Incident Log (Annexure-2)
See also  API Manufacturing: SOP for Water Analysis by KF Titration - V 2.0

8. References

  • ICH Q7 – Good Manufacturing Practice for Active Pharmaceutical Ingredients
  • OSHA Flammable Liquid Transfer Safety Guidelines
  • Company EHS 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: Solvent Transfer Log

Date Solvent Source Vessel Destination Vessel Volume (L) Operator
13/04/2025 Methanol DRM-101 RX-202 120

Annexure-2: Solvent Spill and Incident Log

Date Solvent Location Description Action Taken Reported By
10/04/2025 Acetone Tank Farm Leak from hose clamp Clamp replaced, area cleaned

Revision History:

Revision Date Revision No. Details Reason Approved By
01/01/2022 1.0 Initial Release New Pumping Protocol QA Head
13/04/2025 2.0 Spill Log and Cross-Contamination Precautions Added Audit Feedback QA Head
API Manufacturing V 2.0 Tags:API batch record, API BMR, API calibration, API centrifuge, API cleaning, API crystallization, API deviation, API documentation, API drying, API equipment cleaning, API filtration, API GMP compliance, API granulation, API hold time, API impurities, API line clearance, API manufacturing, API process, API quality control, API reactor, API sampling, API solvent handling, API validation, API waste disposal, API yield

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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
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  • Gels
  • Good Distribution Practice
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  • Injectables
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  • Lotions
  • Lyophilized Products
  • Maintenance Dept.
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  • 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
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