Standard Operating Procedure for Sieving Process in Powders
1) Purpose
The purpose of this SOP is to outline the procedure for conducting the sieving process for powders in the pharmaceutical industry to ensure proper particle size distribution.
2) Scope
This SOP applies to all personnel involved in the sieving process of powders within the pharmaceutical manufacturing department.
3) Responsibilities
Production Operator: Responsible for performing the sieving process.
Quality Control (QC) Analyst: Responsible for verifying the quality aspects related to sieving.
4) Procedure
- Equipment Setup:
- Check and prepare the sieve equipment as per standard operating procedures.
- Verify calibration status of sieves if applicable.
- Sample Preparation:
- Weigh the appropriate amount of sample powder for sieving.
- Ensure sample is representative of the batch and properly labeled.
- Sieving Process:
- Place the sieve stack properly and start the sieving machine.
- Allow the sieving process to continue for the specified duration.
- Visually inspect the sieved material for any clumps or inconsistencies.
- Analysis and Recording:
- Collect the sieved material from each sieve and record the weight retained on each sieve.
- Calculate the particle size distribution based on the weight retained on each sieve.
- Cleaning and Maintenance:
- After sieving, clean the sieves and equipment thoroughly to prevent cross-contamination.
- Maintain records of cleaning and maintenance activities.
5) Abbreviations, if any
SOP: Standard Operating Procedure
QC: Quality Control
6) Documents, if
any
Sieving Process Protocol, Sieve Calibration Records, Sieve Cleaning Log
7) Reference, if any
Pharmacopeial guidelines on particle size distribution testing for pharmaceutical powders.
8) SOP Version
Version 1.0