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API Manufacturing: SOP for Environmental Monitoring in Warehouse – V 2.0

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API Manufacturing: SOP for Environmental Monitoring in Warehouse – V 2.0

Standard Operating Procedure for Environmental Monitoring in Warehouse in API Manufacturing

Department API Manufacturing
SOP No. SOP/API/014/2025
Supersedes SOP/API/014/2022
Page No. Page 1 of 11
Issue Date 13/04/2025
Effective Date 15/04/2025
Review Date 13/04/2026

1. Purpose

To establish a procedure for monitoring and documenting environmental conditions such as temperature, relative humidity, pest control, and cleanliness in API warehouse areas to ensure storage conditions comply with GMP requirements and maintain product quality.

2. Scope

This SOP is applicable to all storage zones within the API manufacturing warehouse including raw material areas, cold rooms, sampling areas, and

quarantine sections.

3. Responsibilities

  • Warehouse Staff: Record temperature and humidity readings daily, report deviations.
  • QA Officer: Review logs, inspect cleanliness, and ensure calibration of instruments.
  • Pest Control Agency: Conduct pest control activities and maintain trap records.
See also  API Manufacturing: SOP for Sample Reconciliation Post IPC Testing - V 2.0

4. Accountability

The Warehouse Manager and QA Manager are accountable for ensuring that environmental monitoring is performed as per this SOP and any deviations are addressed promptly.

5. Procedure

5.1 Temperature and Humidity Monitoring

  1. Install calibrated digital thermohygrometers/data loggers in:
    • General storage area
    • Quarantine area
    • Sampling booths
    • Cold rooms (if applicable)
  2. Record values twice daily (morning and evening) in the “Temperature & Humidity Log” (Annexure-1).
  3. Acceptable limits:
    • Temperature: 15–25°C (unless otherwise specified)
    • Relative Humidity: ≤ 60%
  4. Highlight and escalate any excursions to QA and initiate deviation form.

5.2 Cleanliness Monitoring

  1. Perform daily housekeeping activities including sweeping, mopping, and surface wiping using approved disinfectants.
  2. Record activities in the “Warehouse Cleaning Checklist” (Annexure-2).
  3. QA to inspect cleanliness weekly and sign the verification column.

5.3 Pest Control Monitoring

  1. Contracted pest control agency shall carry out services as per approved schedule (Annexure-3).
  2. Place glue traps/insectocutors at:
    • Entry/Exit Points
    • Storage corners
    • Near drains
  3. Maintain “Pest Monitoring Record” (Annexure-4).
  4. Review and trend the pest count monthly to assess effectiveness.
See also  API Manufacturing: SOP for QC Lab Access and Control Procedure - V 2.0

5.4 Equipment Calibration

  1. Thermometers, hygrometers, and data loggers must be calibrated at least once every 6 months.
  2. Record calibration details in the “Instrument Calibration Log” (Annexure-5).

5.5 Handling Deviations

  1. In case of temperature/humidity deviation:
    • Quarantine affected materials
    • Inform QA for risk assessment
    • Record deviation and corrective action
  2. Initiate CAPA if recurring deviations are observed.

6. Abbreviations

  • SOP: Standard Operating Procedure
  • QA: Quality Assurance
  • CAPA: Corrective and Preventive Action
  • RH: Relative Humidity

7. Documents

  1. Temperature & Humidity Log (Annexure-1)
  2. Warehouse Cleaning Checklist (Annexure-2)
  3. Pest Control Schedule (Annexure-3)
  4. Pest Monitoring Record (Annexure-4)
  5. Instrument Calibration Log (Annexure-5)

8. References

  • ICH Q7 – GMP Guidelines for Active Pharmaceutical Ingredients
  • WHO TRS 961 Annex 9 – Guidelines on Storage and Transport of Time- and Temperature-Sensitive Products
  • 21 CFR Part 211.42 – Environmental control systems

9. SOP Version

Version: 2.0

See also  API Manufacturing: SOP for Change Control Request Evaluation and Implementation - V 2.0

10. Approval Section

Prepared By Checked By Approved By
Signature
Date
Name
Designation
Department

11. Annexures

Annexure-1: Temperature & Humidity Log

Date Time Area Temperature (°C) RH (%) Recorded By
13/04/2025 09:00 RM Store 24.8 57

Annexure-2: Warehouse Cleaning Checklist

Date Area Cleaned Performed By Verified By (QA) Remarks
13/04/2025 Sampling Room —

Annexure-3: Pest Control Schedule

Month Agency Visit Date Activity Performed Remarks
April 2025 PestCare Pvt. Ltd. 05/04/2025 Fogging + Trapping OK

Annexure-4: Pest Monitoring Record

Date Location Trap Type No. of Pests Action Taken
13/04/2025 Quarantine Zone Glue Trap 3 Trap Replaced

Annexure-5: Instrument Calibration Log

Date Instrument ID Calibrated By Next Due Status
01/04/2025 DATA-001 Metrologix Labs 01/10/2025 OK

Revision History:

Revision Date Revision No. Revision Details Reason for Revision Approved By
01/01/2022 1.0 Initial SOP Release New Warehouse Setup QA Head
13/04/2025 2.0 Updated Pest Monitoring and Deviation Handling Audit 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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Next Post: SOP for Identifying and Addressing Moisture Control Issues in Storage – V 2.0

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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