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API Manufacturing: SOP for Storage Conditions for Recovered Solvents – V 2.0

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API Manufacturing: SOP for Storage Conditions for Recovered Solvents – V 2.0

Standard Operating Procedure for Storage Conditions for Recovered Solvents in API Manufacturing

Department API Manufacturing
SOP No. SOP/API/045/2025
Supersedes SOP/API/045/2022
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 required storage conditions for recovered solvents in API manufacturing, ensuring their stability, safety, traceability, and readiness for reuse while maintaining compliance with GMP and environmental regulations.

2. Scope

This SOP applies to all recovered solvents that have been tested and labeled after distillation or purification within the API manufacturing facility and are stored for future reuse or disposal.

3. Responsibilities

  • Warehouse Personnel: Store and monitor recovered solvent containers as per SOP.
  • QA Department: Verify proper labeling and storage compliance.
  • EHS Team: Monitor environmental and safety requirements of solvent storage area.
See also  API Manufacturing: SOP for Pest Control and Monitoring Program - V 2.0

4. Accountability

The Warehouse Manager is accountable for maintaining proper storage conditions. The QA Head is responsible for documentation verification and traceability.

5. Procedure

5.1 Storage Area Requirements

  1. Recovered solvents must be stored in a designated, segregated area marked as “Recovered Solvent Storage.”
  2. The area must be:
    • Well-ventilated
    • Away from direct sunlight and heat sources
    • Equipped with fire protection measures (foam extinguisher, sand bucket)
    • Covered by a roof with proper drainage
  3. Secondary containment trays must be in place to prevent leakage or spills from spreading.
  4. Proper signage for hazardous material handling must be displayed.

5.2 Container and Labeling Control

  1. Only labeled containers as per SOP/API/044/2025 are allowed into storage.
  2. Containers must be:
    • Closed tightly with sealed lids
    • Made of chemically compatible materials (e.g., stainless steel, HDPE)
    • Stored with labels facing outward and legible
  3. Keep separate zones for:
    • Approved for Reuse
    • Rejected Solvents (pending disposal)

5.3 Environmental Monitoring and Control

  1. Record ambient temperature and relative humidity of the storage area daily in the “Storage Condition Monitoring Log” (Annexure-1).
  2. Maintain temperature between 15°C–30°C, unless solvent-specific storage conditions dictate otherwise.
  3. Use flameproof electrical fittings and exhaust ventilation where applicable.
  4. Ensure all solvents are grounded and bonded to prevent static discharge during movement.
See also  API Manufacturing: SOP for Raw Material Sampling Procedure - V 2.0

5.4 Inventory and Movement

  1. Enter each drum or container into the “Recovered Solvent Storage Inventory Register” (Annexure-2).
  2. Log each movement (in/out of the area) and the destination (e.g., recovery, production, disposal).
  3. Ensure FIFO (First In, First Out) or usage based on validity is followed.

5.5 Inspection and Cleaning

  1. Inspect storage drums weekly for any corrosion, leakage, or label fading.
  2. Clean the storage area floor weekly and maintain the “Cleaning Log” (Annexure-3).

6. Abbreviations

  • SOP: Standard Operating Procedure
  • QA: Quality Assurance
  • EHS: Environment, Health, and Safety
  • HDPE: High-Density Polyethylene
  • FIFO: First In First Out

7. Documents

  1. Storage Condition Monitoring Log (Annexure-1)
  2. Recovered Solvent Storage Inventory Register (Annexure-2)
  3. Storage Area Cleaning Log (Annexure-3)
See also  API Manufacturing: SOP for Cleaning Validation Between Batches - V 2.0

8. References

  • ICH Q7 – Good Manufacturing Practice for Active Pharmaceutical Ingredients
  • 21 CFR Part 211 – Subpart C (Buildings and Facilities)
  • WHO TRS 957 – Annex 2 (Environmental Controls)

9. SOP Version

Version: 2.0

10. Approval Section

Prepared By Checked By Approved By
Signature
Date
Name
Designation
Department

11. Annexures

Annexure-1: Storage Condition Monitoring Log

Date Time Temperature (°C) Relative Humidity (%) Checked By Remarks
13/04/2025 09:00 26 55 Within limits

Annexure-2: Recovered Solvent Storage Inventory Register

Date Solvent Batch No. Qty (L) Storage Zone Status
13/04/2025 Acetone RCV-202504 80 Zone A Approved for Reuse

Annexure-3: Storage Area Cleaning Log

Date Area Cleaned Cleaned By Verified By Remarks
13/04/2025 Recovered Solvent Bay No issues

Revision History:

Revision Date Revision No. Details Reason Approved By
01/01/2022 1.0 Initial SOP Release New Regulatory Requirement QA Head
13/04/2025 2.0 Environmental Monitoring Logs Added GMP Compliance 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

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NEW! Revised SOPs – V 2.0

  • Aerosols 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
  • Ointments V 2.0
  • Raw Material Warehouse V 2.0
  • Tablet Manufacturing V2.0

New Publication: A must for All.

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