1.0 Objective:
To provide
written procedure for operation and validation of Laminar Air Flow Hood.
2.0 Scope:
This SOP
covers the operation and validation (in-house) of Laminar Air Flow Hood.
3.0 Responsibility:
Microbiologist: Responsible
for operation, validation and maintenance of the instrument. Maintain the
required record.
QA Officer/QAM: Review the
records and governing the document.
4.0 Procedure:
4.1 Switch on the
mains.
4.2 Switch on the
Ultra Violet light for 30 minutes before beginning of the work.
4.3 Switch on the
Laminar flow at least 15 minutes before beginning of the work.
4.4 Ensure that
Ultra Violet light is off during working period.
4.5 Check the
pressure of Nanometer, lend of the Red liquid indicator. It should be between 5
- 15 mm.
4.6 Record the
Ultra Violet lamp usage and pressure of Nanometer in the Ultra Violet lamp
usage log book
4.7 Switch off the
instrument once the work completed.
4.8 Clean the
interior surface of the Laminar with 70 % IPA before and after the analysis.
5.0 Validation:
5.1 Check the
performance of the HEPA filter by the following methods:
5.1.1 DOP test : To
be performed by external agency.
5.1.2 Particulate
count : To be performed by external
agency.
5.1.3 Velocity
measurement: To be performed by external agency.
Frequency
: Once in a year
5.1.4 Plate count
method:
5.1.4.1 Expose Soya bean casein digest agar and Sabouraud Chloramphenicol Agar plates (in
duplicate) to air flow for 2
hours.
5.1.4.2 Incubate Soya bean Casein Digest Agar plate at
35- 37° C for 24 hours and Sabouraud
Chloramphenicol Agar plate at 20-25° C for 72 to 120 hours.
5.1.4.3 Observe the plate
and count the no. of colonies found. Record the observations in the Laminar flow validation log book
5.1.4.4 Acceptance
Criteria: Not more than 1 cfu per
plate/2 hour.
5.1.4.5 Frequency: Once in a month.
6.0
Routine maintenance:
6.1
Clean the instrument with dry
cloth and LAF bench with Isopropyl alcohol.
6.2
Check the level of the red
liquid.
6.3
Clean the tube of ultraviolet
light with dry cloth.
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