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SOP Guide for Pharma

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SOP for proper storage of received goods

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Standard Operating Procedure of Storage of Received Material

Purpose

The purpose of this SOP is to establish guidelines for the proper storage of pharmaceutical products to maintain their integrity, efficacy, and safety throughout their shelf life.

Scope

This SOP applies to all storage areas within the pharmaceutical facility where pharmaceutical products are stored, including warehouses, cold rooms, and controlled storage areas.

Responsibilities

  • Warehouse Manager: Responsible for overall implementation and compliance with storage SOP.
  • Quality Assurance (QA) Department: Responsible for periodic inspections to ensure compliance with storage conditions.
  • Warehouse Staff: Responsible for adhering to storage guidelines and reporting any deviations or issues.
See also  SOP for Hygiene Practices

Procedure

  1. Temperature Control: Maintain temperature within specified ranges as per product requirements. Monitor temperature regularly using calibrated thermometers.
  2. Humidity Control: Maintain humidity levels within acceptable limits to prevent moisture-related damage to products. Use dehumidifiers if necessary.
  3. Storage Organization: Store pharmaceutical products according to their storage requirements, including segregation of different temperature-sensitive products.
  4. Security Measures: Implement security measures such as access controls, CCTV surveillance, and restricted access to authorized personnel only.
  5. Documentation: Maintain accurate records of temperature and humidity logs, including any deviations or corrective actions taken.
  6. Cleaning and Maintenance: Regularly clean and maintain storage equipment and facilities to prevent contamination and ensure proper functioning.
  7. Emergency Preparedness: Develop and implement procedures for addressing emergencies such as power outages, equipment failures, or environmental hazards.
  8. Training: Provide training to warehouse staff on storage SOPs, including proper handling and storage practices.
See also  SOP for Restricted Area Access

Abbreviations

  • SOP: Standard Operating Procedure
  • QA: Quality Assurance
  • CCTV: Closed-Circuit Television

Documents

  • Temperature and humidity logs
  • Training records
  • Emergency procedures manual

Reference

Pharmaceutical Storage and Distribution Guidelines (if applicable)

SOP 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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