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

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 on Raw Material Sampling Plan Procedure

Posted on By

1. Purpose
The purpose of this standard operating procedure (SOP) is to provide guidance on the raw material sampling plan procedure. This SOP outlines the process of sampling and testing raw materials to ensure they meet the required quality standards for use in the manufacturing process.

2. Scope
This SOP applies to all staff involved in the raw materials sampling process.

3. Responsibilities
The following personnel are responsible for ensuring compliance with this SOP:
– Production Manager
– Quality Control Manager
– Laboratory Technician
– Raw Material Warehouse Supervisor

4. Materials Required
– Sampling equipment (such as scoops, spoons, or pipettes)
– Labels
– Marker pens

See also  SOP on Raw Material Transportation Procedure

5. Sampling Process
5.1. Sample Size
– The size of the sample taken should be large enough to be representative of the entire lot.
– The recommended sample size as per regulatory guidelines is at least 5% of the lot size.
– The minimum sample size should be 200 grams.

Number of containers to be sampled is as follows:

For containers upto 5 : All containers.

For containers above 5: √n +15

.2. Sampling Procedure

– The Sampling procedure should be conducted only by trained personnel who follow proper hygiene procedures.
– The samples should be taken from at least 10

different points in the lot, at various depths, and locations, in a random manner.
– The samples should be taken from different containers or sacks from the lot.
– The samples should be taken from the middle of the lot avoiding the top or bottom layer where separation can occur.

See also  SOP on Raw Material Quarantine Procedure

5.3. Sample labeling and documentation
– Samples should be labeled with the lot number, date of sampling, name of the sampler, Sampling point identification number.
– The labeling should be precise, clear, and durable enough for the entire sampling and testing process.
– Samples should be documented with the relevant data such as name of the supplier, date of receipt, expiry date, Certificate of Analysis (COA) of the raw material.

5.4. Transport and Storage of Samples
-The samples should be transported to the laboratory for testing as soon as possible to avoid any deterioration.
– The samples should be kept in well-labeled sample containers and tightly sealed, and stored away from direct sunlight, moisture, and extremes of temperature.
– Samples should be stored at the recommended temperature and duration as per SOP.

See also  Raw Material Sampling Plan: Procedure for Water Sampling

6. Conclusion
By following this Raw Material Sampling Plan Procedure SOP, the organization can ensure consistent and reliable quality of raw materials for manufacturing and provide assurance to customers that they are receiving safe and compliant products.

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 on Raw Material Transportation Procedure
Next Post: SOP on Raw Material Retention 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