Skip to content
  • Clinical Studies
  • Pharma GMP
  • Pharma Tips
  • Stability Studies
  • Pharma Books
  • Schedule M

SOP Guide for Pharma

The Ultimate Resource for Pharmaceutical SOPs and Best Practices

  • Home
  • Job Safety Analysis (JSA)
    • Oral Dosage Forms (Tablets & Capsules)
    • Oral Liquid Dosage Forms (Syrups, Elixirs, Suspensions, Emulsions)
    • Powder and Granule Dosage Forms
    • Topical Dosage Forms (Creams, Ointments, Gels, Lotions, Pastes)
    • Transdermal Dosage Forms (Patches)
  • Standard Test Procedures (STP)
  • SOP – Blog Post
  • Toggle search form

SOP for Raw Material Expiry Date Management Procedure

Posted on By

1. Purpose:
The purpose of this SOP is to establish a procedure for the effective management of raw material expiry date to ensure that materials are used within their shelf life.

2. Scope:
This procedure applies to all raw materials used in the production processes at the company.

3. Responsibilities:
a. Procurement Department: Responsible for verifying the expiry date of all materials before purchase and ensuring that materials with a shelf life of less than six months are not purchased.
b. Warehouse Department: Responsible for proper storage of materials in accordance with storage requirements and ensures that materials with less than six months’ shelf life are labelled and stored in a separate area.
c. Production Department: Responsible for verifying the expiry date of all materials before use andcc ensuring that no expired materials are used in the production processes.
d. Quality Assurance Department: Responsible for verifying the expiry date of all materials before use and conducting regular inspections of the storage area to ensure that all materials are stored under the required conditions.

See also  SOP for Raw Material Testing Procedure

4. Procedure:
a. The procurement department shall verify the expiry date of all materials before purchase. Materials with a shelf life of less than six months should not be purchased.

/> b. The warehouse department shall ensure that all materials are stored in accordance with the required conditions, and any materials with less than six months’ shelf life should be labelled and stored in a separate area.
c. The production department shall verify the expiry date of all materials before use, and no expired materials should be used in the production processes.
d. The quality assurance department shall ensure that all departments comply with this SOP and conduct regular inspections of the storage area to ensure that all materials are stored under the required conditions.
e. The warehouse department shall ensure the proper disposal of all expired materials.

See also  SOP on Raw Material Handling Record Procedure

5. Abbreviations:
N/A

6. Documents:
a. Material Purchase Order
b. Material Inspection Report
c. Material Storage Report

7. Reference:
N/A

8. SOP Version: 1.0

Raw Material Stores Tags:Efficient workflow in raw material stores, Quality control procedures for raw materials, Raw material SOP, Raw material store management, Raw material store SOP, SOP for raw material stores, SOP of raw material stores, Standard Operating Procedures for raw materials

Post navigation

Previous Post: SOP for Raw Material CoA Retention Procedure
Next Post: SOP for Raw Material Rejection Procedure

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

Read SOPs in your Language:

 - 
Bengali
 - 
bn
English
 - 
en
Gujarati
 - 
gu
Hindi
 - 
hi
Malayalam
 - 
ml
Marathi
 - 
mr
Punjabi
 - 
pa
Tamil
 - 
ta
Telugu
 - 
te

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.

Copyright © 2025 SOP Guide for Pharma.

Powered by PressBook WordPress theme

Go to mobile version