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SOP Guide for Pharma

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SOP for Storage Conditions of Powders

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SOP for Storage Conditions of Powders

Standard Operating Procedure for Storage Conditions of Powders

1) Purpose

The purpose of this SOP is to define the standard storage conditions for powders in the pharmaceutical industry to maintain their stability and quality throughout their shelf-life.

2) Scope

This SOP applies to all personnel involved in the storage of powders within the pharmaceutical manufacturing facility.

3) Responsibilities

Warehouse Personnel: Responsible for implementing and monitoring storage conditions.
Quality Assurance: Responsible for ensuring compliance with storage requirements.
Production Managers: Responsible for coordinating storage activities.

4) Procedure

  1. Storage Area Identification:
    1. Designate specific areas within the warehouse for powder storage.
    2. Ensure areas are clean, dry, and free from potential contaminants.
  2. Temperature and Humidity Control:
    1. Set and monitor storage temperatures as per product specifications.
    2. Maintain humidity levels within acceptable limits to prevent degradation.
  3. Light Protection:
    1. Store powders away from direct sunlight and artificial light sources that may degrade sensitive compounds.
    2. Use light-resistant containers or coverings when necessary.
  4. Storage Conditions Monitoring:
    1. Regularly monitor and record storage temperatures and humidity levels.
    2. Document any deviations from specified conditions and take corrective actions promptly.
  5. Security and Access Control:
    1. Implement security measures to prevent unauthorized access to stored powders.
    2. Ensure only authorized personnel have access to the storage areas.
  6. Documentation:
    1. Maintain accurate records of storage conditions, including temperature logs and humidity records.
    2. Review and archive records as per document retention policies.
See also  SOP for Assay of Active Ingredient in Powders

5) Abbreviations, if any

SOP: Standard Operating Procedure
GMP: Good Manufacturing Practice

6) Documents, if any

Storage Area Mapping, Temperature and Humidity Logs

7) Reference, if any

ICH guidelines and pharmaceutical storage requirements.

8) SOP Version

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

New Publication: A must for All.

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