HEPA Filters for Pharma Applications

Transcription

HEPA Filters for Pharma Applications
HEPA Filters for Pharma
Applications – Cleanrooms &
Safety Applications
Gordon Farquharson
June 2012
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Air Filters at work
Images courtesy of CamfilFarr
2
How filters work
Sieving Effect
Straining
3
Filter Test Methods
4
Filter
Specifications
5
Some important filter considerations
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Correct pre-filters protect systems
& prolong life of final filters
HEPA filters are required in
cleanroom & safety ventilation
applications
Designs and installation must
allow for convenient & safe
filter testing
Make sure you know what filters
are installed in the system
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HEPA Filter Standards
HEPA Filters are dealt with
in 4 basic ways.
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Filter Construction standards
Factory or manufacturer’s tests
In-situ testing of installations
Some application standards include HEPA Filter
specifications (e.g. EN 12469 for Biosafety Cabinets)
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Filter Test Methods
MPPS = 0.2 
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Some Test Equipment
Thermo-Pneumatic Aerosol Generator
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Some Test Equipment
Laskin Nozzle
Cold Generator
10
Some Test Equipment
Aerosol Photometer
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New Standards from
CEN TC 195 - Air Filtration 2
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EN 1822-3 Testing
Planar Filter Medium
to determine the
MPPS -- Most
Penetrating Particle
size. The processes
of Interception,
Diffusion & Straining
give the following
classic curve.
Performance is
velocity dependent.
HEPA & ULPA Filters
v1
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HEPA & ULPA Filters
EN 1822 - Factory Test
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EN 1822 compared with
Eurovent 4/4 NaCl
Eurovent 4/4
EN 1822
Filter Class Efficiency % Filter Class Efficiency %
H 10
85
H 11
95
EU 10
95 - 99.9
H 12
99.5
EU 11
99.9 – 99.97
EU 12
99.97 – 99.99 H 13
99.95
EU 13
99.99– 99.999
H 14
99.995
EU 14
> 99.999
U 15
99.9995
U 16
99.99995
U 17
99.999995
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EN 1822-1 Filter Classifications
Local efficiency = 5x 0verall
H 10
H11
H12
H13
H14
U15
U16
U17
Overall Effic/Pen Local Effic/Pen
85 / 15 %
na / na
95 / 5
na / na
99.5 / 0.5
na / na
99.95 / 0.05
99.75 / 0.25 %
99.995 / 0.005
99.975 / 0.025
99.9995 / 0.0005
99.9975 / 0.0025
99.99995/0.00005
99.99975 / 0.00025
99.999995/0.000005 99.9999 / 0.0001
To avoid problems with In-situ test, always
specify a face scanned filter from the supplier !
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Local & Overall Efficiency
H 14 example
@ MPPS
Local pen
< 0.025 %
Local & Overall
Pen % must pass
Local pen
< 0.025 %
Local pen
< 0.025 %
Overall penetration
< 0.005 % @ MPPS
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Leak test In-situ
PAO test
Local pen
< 0.01 %
Local pen
< 0.01 %
Local pen
< 0.01 %
Overall penetration
< 0.001 or 0.003 % @ MPPS
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Local & Overall Efficiency
H 14 example
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How do we choose our HEPA filters ??
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From the requirements in a Cleanroom Standard or GMP
rule/guideline.
Because we have chosen a certain acceptance value for
the In-Situ leak test e.g. 0.001% or 0.01% .
Because we have calculated the efficiency of filter we need
from an evaluation of the particle challenge imposed upon
the filters.
Because the filter gives good Uni-Directional Flow.
Compliance with some other requirement
e.g. Corporate.
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Choosing the Right
http://www.phss.co.uk/
HEPA Filter
EU GMP Grade
A
Class
At Rest
14644-1 209E
 0.5 
ISO 5
100
M3.5
Class
In Operation
14644-1 209E
 0.5 
Air flow regime
and final filter
configuration
ISO 5
100
M3.5
UDAF
Terminal HEPA
filter
ISO 7
B
ISO 5
100
M3.5
10,000
M5.5
N-UDAF
Terminal HEPA
filter
C
ISO 7
10,000
M5.5
ISO 8
100,000
M6.5
N-UDAF
Terminal HEPA
filter
D
ISO 8
100,000
M6.5
Not defined
N-UDAF
In plant final filter
Final Filter
In situ test leak test
specification to
method
EN 1822
U15
H14
Face scan with
aerosol &
photometer
0.001 %
0.01 %
H14
Face scan with
aerosol &
photometer
0.01 %
H14
Face scan with
aerosol &
photometer
0.01 %
Volumetric overall
penetration.
0.01 %
H13
Refers to filter grades in accordance with EN 1822 ULPA , & HEPA
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Test
acceptance
criteria =
stated %
The Installed HEPA Filter
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Typical Aseptic Facility Design
(From ISPE HVAC GPG)
Outside air
treatment
AHU
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In-Situ Testing General
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Select test method, aerosol, and acceptance
criteria
Determine challenge up-stream
Scan test final filter face for leaks
Determine acceptance or rejection
Carry out remedial work.
Agree before repairing filters. Have a clear policy.
ISO 14644-3 allows repair, subject to manufacturer’s
approved method.
I don’t know any manufacturers who encourage repairs.
Re-test
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Testing is application specific
Filter testing in this Isolator
is a different problem from
the cleanroom.
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Filter Systems for Potent,
Toxic, Biohazard
applications
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Exposure Control Potent
Compound Control Bands
EH & S
Call the shots!
EXPOSURE CONTROL BAND
Band
OEL Range
Design
1
>1000 ug/m3
General Ventilation, Conventional open Equipment
with local exhaust (LEV)
2
50-1000 ug/m3
Semi-closed to closed materialo transfer
laminar flow/directionalized laminar flow
engineered LEV
3
20-50 ug/m3
Transfers using direct couplings % closed systems
selected use of unidirectionalized air flow booths
4
1-20 ug/m3
Totally enclosed processes: Transfers using direct
coupling barrier/isolator technology
5
<1 ug/m3
Isolator technology; remote operations fully
auotmated
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Typical OSD Facility
Using Multiple Air handlers (From ISPE HVAC GPG)
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BIBO (Bag-In, Bag-Out Housing
Fully Self contained system with fan, integrated
dampers & automatic scan section optional
Cover Panel
Access door for BT damper
Scan section
Hepa Section
Pre filter section
Air intake
levelling feet
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Filter Leak Test Procedure!
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Duct mounted double exhaust
housing
Safety ventilation systems - typical contemporary BSL-3
exhaust system
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High Total
Cost of
Ownership
Large
Each system
must be
specifically
oriented
Costly to test
Typical BSL-3 HEPA Filter
Exhaust System
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High Efficiency Particulate Air
(HEPA) Filter
Field system leak testing – manual
scanning
Potential Risk to
Certifier
 Requires lab shutdown
and system
decontamination
 Slow process
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Field system leak testing – automated
scanning
Control Unit
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Conclusions
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Be aware of the Different Standards
Understand the configuration
Specify filters correctly (including leak testing)
Install carefully
Test In-situ
Plan re-testing
Keep records
Thanks for your attention Questions?
37
PharmOut
Unit 20, 40 Montclair Avenue,
Glen Waverley,
Victoria,
Australia, 3150
Tel +61 (0) 3 8610 0169
Thanks for your attention
Slid
e 38
S
Y
S
CRITICAL
E
M
S
Gordon J Farquharson
Chair BSI LBI/030; Chair CEN TC243; Convenor ISO TC209 WG1.
c/o Critical Systems Ltd
www.critical-systems.co.uk
4, Greencroft, Guildford,
Surrey, GU1 2SY, UK.
tel +44 (0)1483 579926
mob +44 (0)7785 265 909
e-mail [email protected] & [email protected]
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