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 Dispensing Procedure

Posted on By

Title: Raw Material Dispensing Procedure

1.0 Objective:
To ensure that the raw materials are dispensed accurately, safely, and efficiently for production.

2.0 Scope:
This procedure covers the process of dispensing raw materials for use in production processes.

3.0 Responsibility:
The production supervisor is responsible for ensuring that the raw materials dispensing procedure is followed by the production team.

4.0 Procedure:

4.1. Raw material receipt and storage:
Raw materials are received and stored in designated areas according to the manufacturer’s instructions and GMP guidelines.

4.2. Batch planning:
The production supervisor must ensure that the required raw materials have been approved for use in the specific production batch based on the batch record.

See also  SOP for Raw Material Verification Procedure

4.3. Preparation of dispensing area:
The dispensing area must be clean and sanitized, free from any residue from the previous batch. All necessary equipment and measuring devices should be checked and calibrated before use.

4.4. Weighing:
The production team shall accurately weigh the required raw materials as per the batch record. The team must follow instructions carefully to ensure that the correct quantity of each raw material is dispensed.

4.5. Labeling:
Each raw material must be labeled with its name, batch number, and quantity to ensure proper identification and tracking throughout the production process.

4.6. Reconciliation:
At the end

of each dispensing process, the production team must reconcile the amount of material dispensed with the amount required to ensure that all raw materials have been dispensed correctly.

See also  SOP for Raw Material Non-conformance Procedure

4.7. Return and quarantine:
Any unused raw material must be returned to the designated storage area and appropriately labeled before being quarantined for use in future batches.

4.8. Sanitation and cleaning:
The dispensing area, equipment, and tools must be cleaned and sanitized after each dispensing process to prevent contamination and ensure cleanliness.

5.0 Conclusion:
The Raw Material Dispensing Procedure is essential for accurate, safe, and efficient production. Following this procedure will help ensure that high-quality products are consistently produced.

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 Operation of Vernier Caliper
Next Post: SOP for Raw Material Handling 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