STANDARD OPERATING PROCEDURE Disposal of Used Media and Cultures
STANDARD OPERATING PROCEDURE |
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Department: Quality Control
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SOP No.: QC/MB/xxx
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Disposal of Used Media and Cultures
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Effective
Date:
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Review
Date:
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Page
No.: 1
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1.0
OBJECTIVE:
1.1
To lay down a procedure for destruction and disposal of used media and cultures.
2.0
SCOPE:
2.1
This Procedure is applicable for
destruction and disposal of the used media and cultures in Microbiology laboratory
at Private Limited.
3.0
RESPONSIBILITY:
3.1
Lab Assistant: Performing the destruction activity
3.2
Microbiologist- Execution of activity
3.3
Section In-charge – To review the activity and check the records
3.4
QC Head- To implement the Procedure
3.5
Head QA- Overall Compliance
4.0
PROCEDURE:
4.1
For Conical Flasks and Test Tubes:
4.1.1
Place the used media conical flasks, test
tubes, positive control flasks and culture suspension test tubes in a stainless
steel container.
4.1.2
Keep the loaded stainless steel container
in autoclave and sterilize at 15 lbs. pressure, at 121°C temperature for 30
minutes.
4.1.3
Record the load details in Annexure I of
QC/MB/059 or Annexure II of QC/MB/045.
4.1.4
After competition of autoclave cycle, take
the stainless steel container to the washing area, remove the sterilized
conical flasks and test tubes from the stainless steel container.
4.1.5
Collect the liquid media or broth from
conical flasks and test tubes into a polythene cover send to effluent tank.
4.1.6
Now keep the empty tubes and conical flasks
in any of disinfectant (5 % v/v Dettol, 5% v/v Savlon, 1% v/v Bacillocid
special or 1% Hospal –OT) solution for 1 hour and follow further cleaning
procedure as per the current version of SOP No.: QC/MB/016.
4.2
For
Glass petri plates and culture slants:
4.2.1
Place the used glass petri plates, culture
slants (test tubes) and positive control plates in a stainless steel container.
4.2.2
Keep the loaded stainless steel container
in autoclave and sterilize at 15 lbs. pressure, at 121°C temperature for 30
minutes.
4.2.3
Record the load details in Annexure I of
QC/MB/059 or Annexure II of QC/MB/045.
4.2.4
After competition of autoclave cycle, take
the stainless steel container to the washing area, remove the sterilized petri
plates and culture slants from the stainless steel container.
4.2.5
Collect the molten agar media from petri
plates and culture slants (test tubes) into a polythene cover send to effluent
tank.
4.2.6
Now keep the empty plates and test tubes
in any of disinfectant (5 % v/v Dettol, 5% v/v Savlon, 1% v/v Bacillocid
special or 1% Hospal –OT) solution for one hour and follow further cleaning
procedure as per the current version of SOP No.: QC/MB/016.
4.3
For Disposable petri
plates:
4.3.1
Remove the used agar media from disposable petri plates and
collect into disposable autoclavable poly bags.
4.3.2
Collect all empty disposable petri plates in to another
autoclavable poly bag.
4.3.3
Place the media filled autoclavable poly
bags and empty petri plates filled autoclavable poly bags in a stainless steel container.
4.3.4
Keep the loaded stainless steel container
in autoclave and sterilize at 15 lbs. pressure, at 121°C temperature for 30
minutes.
4.3.5
Record the load details in Annexure I of
QC/MB/xxx or Annexure II of QC/MB/xxx.
4.3.6
After competition of autoclave cycle, take
the stainless steel container to the washing area, remove the sterilized petri
plates poly bags and media poly bag from the stainless steel container.
4.3.7
Send the sterilized media to effluent tank and sterilized
disposable petri plates to scrap.
4.4
Precautions:
4.4.1
Wear nose mask and hand gloves before starting the destruction activity.
4.4.2
Use heat-proof gloves, nose mask &
goggles during handling of sterilized disposable material.
5.0
ABBREVIATIONS:
QC: Quality Control
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QA: Quality Assurance
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v/v:
Volume / Volume
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%: Percentage
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SOP:
Standard Operating Procedure
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6.0
ANNEXURES : NA
7.0
REFERENCES:
7.1
Methods for the collection and analysis of aquatic biological
and microbiological samples:
Britton, L.J., and Greeson, P.E., 1987, Page no. 39 and 53.
7.2
World Health Organization WHO Technical Report Series, No. 961, 2011
Annex 2, (WHO good practices for pharmaceutical microbiology laboratories).
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