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SOP for Microbiological Testing of Raw Materials, Packing Material, Finished Product & Stability Samples

OBJECTIVE
To lay down a procedure for the microbiological testing of raw materials, packing material, finished product and stability samples.

SCOPE
This procedure is applicable to microbiological testing of raw materials, packing materials, finished products and stability samples.

RESPONSIBILITY
Microbiologist – Responsible for analysis and reporting the results.
Section in-charge – Responsible for review the activity and results.
QC Head – Responsible for implementing the Procedure.
QA Head – Overall compliance.

PROCEDURE
  • After receiving the samples of packing materials, raw material, finished and stability entry shall be done in respective inward registers.
  • Raw materials and packing materials shall be entered in Annexure I (Raw Material inward register).
  • Finished Products and Stability samples shall be entered in Annexure II (Finished Products inward register).
  • Allotment of M.R. No. shall be MX-R/YYZZZ, 
Where,
M stands for micro, 
X stands for material (raw material, packaging material
R, Finished product, Stability, Blending, core, coated, packing strips 
YY stands for academic year, 
ZZZ -sequential number starting from 001 for respective material.

  • Preparation of microbial media: Prepare and sterilize the required media as per current version of SOP (Preparation and sterilization of Microbial Media).
  • The material shall be tested for Total Aerobic Microbial Count (TAMC), Total Yeast & Mold Count (TYMC) and Test for specified micro-organisms as per pharmacopeia status and specification.
  • Analysis shall be carried out as per current version of general test procedure.
  • After Completion of microbial analysis certificate of analysis shall be made as per finished product / raw material specification.
  • Raw data for microbiological analysis for raw materials and packing materials, finished products, and stability samples shall be written in Annexure IV.
  • Microbiological Test report for raw materials, packing materials, finished products, and stability samples shall be prepared in Annexure III.
  • If any sample is positive for any specified micro-organism, perform the confirmatory test.
  • The results of the confirmatory tests shall be recorded in Annexure VI.
  • If any results fail to meet specification, an out of specification shall be carried out as per current version of SOP.

ABBREVIATIONS
QC: Quality Control
QA: Quality Assurance
SOP: Standard Operating Procedure
MB: Microbiology

REVISION HISTORY
Nil

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