SOP for Validation of Autoclave with Biological Indicator for Sterilization Efficiency | Pharmaguideline
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  • Apr 17, 2021

    SOP for Validation of Autoclave with Biological Indicator for Sterilization Efficiency

    Standard operating procedure to validate the Autoclave using Biological Indicators for sterilization efficiency.

    1.0 OBJECTIVE

    To describe the procedure to validate autoclave with the biological indicator for sterilization efficiency.

    2.0 SCOPE

    This is applicable to validate autoclave with the biological indicator for sterilization efficiency.

    3.0 RESPONSIBILITY

    Microbiologist - Quality Control

    4.0 ACCOUNTABILITY

    Manager - Quality Control.

    5.0 PROCEDURE

    5.1 Frequency –Monthly
    5.2 Organism – Bacillus stearothermophilus.
    5.3 Perform the initial count of one strip of Bacillus stearothermophilus spores from the strips of given lot/ batch which are to be used for validation purpose.

    5.4 Autoclave validation

    5.4.1 Load the autoclave chamber with routine accessories and glassware.
    5.4.2 Take three strips and mark with location and put inside the autoclave as described below.
    5.4.3 Put one strip in the inner side, one side in middle and one strip outer side, near the door of the autoclave chamber.
    5.4.4 Keep one strip unexposed for + ve control.
    5.4.5 Run the autoclave cycle at 121ยบC and 15 lb pressure for 20 minutes/validated time.
    5.4.6 Mark the pre-incubated sterile SCDM (Soybean Casein Digest Medium) tubes (20ml) with location no., date etc. and transfer the strips aseptically to respective labeled SCDM tubes.
    5.4.7 Transfer one unexposed for + ve control.
    5.4.8 Keep one SCDM tube un-inoculated for – ve control.
    5.4.9 Incubate all the tubes at 55ยบC- 60ยบC for 7 days.
    5.4.10 Observe the tubes daily up to 7 days for turbidity/ growth in the SCDM tubes having strips.
    5.4.11 Positive control should show growth within 72 hours.

    5.5 Interpretation

    5.5.1 If no growth observed in any one of the SCDM tube having autoclaved strips, test complies.
    5.5.2 If growth observed in any one of the SCDM tube, identity the growth of B. stearothermophilus performing gram staining, simultaneously comparing it with + ve control. In case of failure, investigate for non-compliance of validation and repeat the cycle.
    5.5.3 Inform the QC manager /engineering dept. for corrective action.

    6.0 ABBREVIATIONS

    6.1 SOP - Standard Operating Procedure
    6.2 SCDM - Soybean Casein Digest Medium

    ANNEXURE –I
    AUTOCLAVE VALIDATION WITH BIOLOGICAL INDICATOR
    Asset ID  No.
    :

    Ref.  SOP No.
    :

    Make
    :

    Model No.
    :

    Organism used: Bacillus stearothermophilus
    Lot No:------------------------------------
    Date of Sterilization --------------------               Exp. Date -----------------------------------
    Date of completion ----------------------             Population ---------------------------------
    Location
    Growth of Bacillus stearothermophilus observed (+ve) /not observed (-ve) 55-60 °C
    Remarks
    1








    2








    3








    Date








    Observed by








    Observation: The Autoclave is working satisfactorily /not working satisfactorily, requires/does not require maintenance.
    Analyst                                                                                                     Checked by
    Date                                                                                                         Date
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