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SOP for Storage Conditions of Lotions

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SOP for Storage Conditions of Lotions

Standard Operating Procedure for Storage Conditions of Lotions

1) Purpose

The purpose of this SOP is to define the appropriate storage conditions for lotions to maintain their stability, integrity, and efficacy throughout their shelf life.

2) Scope

This SOP applies to all personnel involved in the handling, storage, and distribution of lotions within the pharmaceutical manufacturing facility.

3) Responsibilities

The responsibilities for executing this SOP are as follows:

Warehouse Personnel:

  • Ensure lotions are stored according to the specifications outlined in this SOP.
  • Monitor storage conditions regularly to maintain compliance.
See also  SOP for Formulation Development for Lotions

Quality Control Personnel:

  • Verify that storage conditions comply with regulatory requirements and product specifications.
  • Monitor environmental conditions in storage areas.

Quality Assurance Personnel:

  • Ensure that the storage conditions are documented and reviewed regularly.
  • Investigate and address any deviations from specified storage conditions.

4) Procedure

4.1 General Storage Conditions:

  • Store lotions in a dedicated area that meets the specified environmental conditions (temperature, humidity, light exposure).
  • Ensure storage areas are clean, dry, and free from contaminants.

4.2 Specific Storage Conditions:

  • Temperature: Store lotions at the specified temperature range, typically between 15°C to 25°C, unless otherwise specified by product stability data.
  • Humidity: Maintain humidity levels within acceptable limits to prevent moisture absorption or loss.
  • Light Exposure: Protect lotions from direct sunlight or artificial light sources that could degrade sensitive ingredients.
  • Container Integrity: Ensure
lotions are stored in tightly sealed containers to prevent contamination and maintain product integrity.

4.3 Monitoring and Documentation:

  • Regularly monitor and record storage conditions, including temperature and humidity levels.
  • Document storage conditions in the designated logbook or electronic system.

4.4 Handling Procedures:

  • Follow proper handling procedures when retrieving lotions from storage to prevent damage or contamination.
  • Use FIFO (First In, First Out) method to ensure older stock is used first.

5) Abbreviations, if any

FIFO: First In, First Out

6) Documents, if any

  • Storage Condition Logbook
  • Product Stability Data

7) Reference, if any

  • ICH Q1A(R2): Stability Testing of New Drug Substances and Products
  • USP General Chapter <1079>: Good Storage and Distribution Practices

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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