1.1 To lay down a procedure for Microbiological Testing of Raw materials, Finished products and Intermediates.
2.0 SCOPE
2.1 This procedure applies to the Pharmaceutical Manufacturing Facility of __________________________________________________________________
3.0 RESPONSIBILITY
3.1 Microbiologists.
4.0 ACCOUNTABILITY
4.1 Head-Quality control
5.0 PROCEDURE
5.1 Total Viable Aerobic Microbial Count:
5.1.1 Pretreatment: For freely soluble samples:
5.1.1 Dissolve or suspend 10 g or 10 ml of the sample to be examined in 90ml of sterile Lactose broth media with 0.1% Twin 80.
5.1.2 For samples with antibiotics:
5.1.2.1 Dilute or dissolve 10gm or 10 ml of the sample in 90 ml of sterile Lactose broth media with 0.1% Twin 80.
5.1.3 For poorly wet table samples:
5.1.3.1 Dilute or dissolve 10gm or 10 ml of the sample in 90 ml buffered sodium Chloride peptone pH 7.0 + 0.1% of w/v of polysorbate 80 to solution.
5.1.4 Membrane filtration Method & Pour plate method:
5.1.4.1 Refer GTP.No.:.........
5.1.4.2 Limits: as per individual monograph
5.1.5 For specified Micro organisms.
5.1.5.1 Sample examined to be free from following pathogens as per individual monograph:
5.1.5.2 Escherichia coli.
5.1.5.3 Enterobacteria
5.1.5.4 Salmonella sp.
5.1.5.5 Staphylococcus aureus.
5.1.5.6 Pseudomonas aeruginosa.
5.1.5.7 Refer GTP.No.:..........
5.1.6 Frequency Of Operation:
5.1.6.1 Raw material : As per monograph
5.1.6.2 Finish product: First three batches and every tenth batch or as per requirement.
6.0 ABBRIVIATIONS
6.1 GTP : General Testing Procedure
7.0 REFERENCES
7.1 NIL
8.0 ANNEXURES
8.1 Annexure –I : Total viable aerobic microbial count and specified microorganism test report.
END OF THE DOCUMENT
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