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Continuous Particle Monitoring

1) The document discusses best practices for continuous particle monitoring in pharmaceutical clean rooms, including recommended monitoring frequencies, sample volumes, clean up periods, and how to account for particle loss in tubing. 2) It provides guidelines for monitoring different clean room grades, with mandatory monitoring recommended for Grade A areas. Sample size should be sufficient to capture transient events rather than requiring 1 m3 samples. 3) Risk analysis is recommended to determine optimal monitoring locations, with examples provided. Alert and action limits should be set based on statistical analysis of particle count data from normal production.

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36 views

Continuous Particle Monitoring

1) The document discusses best practices for continuous particle monitoring in pharmaceutical clean rooms, including recommended monitoring frequencies, sample volumes, clean up periods, and how to account for particle loss in tubing. 2) It provides guidelines for monitoring different clean room grades, with mandatory monitoring recommended for Grade A areas. Sample size should be sufficient to capture transient events rather than requiring 1 m3 samples. 3) Risk analysis is recommended to determine optimal monitoring locations, with examples provided. Alert and action limits should be set based on statistical analysis of particle count data from normal production.

Uploaded by

hagg
Copyright
© © All Rights Reserved
Available Formats
Download as PDF, TXT or read online on Scribd
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Best Practice for Continuous Particle

Monitoring in Pharmaceutical Clean Rooms

PDA Europe Conference


June 2010
Jrg Dressler
PMT GmbH
[email protected]

1
Abstract

Presentation touches the most common user questions


regarding interpretation of Annex 1:

Monitoring frequencies

Sample volumes for monitoring

Clean up period

Particle loss in tubing

Sample points via risk analysis

How to define limits

2
Documents to be discussed
CLEAN ROOM AND CLEAN AIR DEVICE CLASSIFICATION

The maximum permitted airborne


concentration for each grade is given in the following table:
Max. Particle Concentration (per m3)

AT REST IN OPERATION
Grades 0,5 m 5,0 m 0,5 m 5,0 m
A 3.520 20 (ISO 4,8) 3.520 20
B 3.520 29 352.000 2.900
C 352.000 2.900 3.520.000 29.000
D 3.520.000 29.000 nA nA

These limits apply for clean room classification.


They do not automatically apply for monitoring sample points.
Monitoring limits will be discussed later.
MICROBIAL MONITORING

limits for microbial contamination (a)


Volumetric Settling plates Contact plates
sampling (D= 90 mm) (D= 55 mm)
(cfu/m3) cfu / 4 hr (b) cfu / plate
Grades
A < 1 < 1 < 1
B 10 5 5
C 100 10 25
D 200 100 50

(a) Average values


(b) Individual settling plates < 4 hrs
CLEAN ROOM ... MONITORING

In Grade A areas monitoring is mandatory

For grade A zones, particle monitoring should be undertaken


for the full duration of critical processing ...

Getting a complete picture is mandatory too

Grade A zones should be monitored at a frequency and with


suitable sample size that all interventions, transient events,
and any system deterioration can be captured
Example - 48 hrs 0,5 um data - A area

#1

#2
Catching the transient events example # 1

Total event covers 2298 counts

Measurement over 35 minute


would give 2298 counts/m3
Analysing the 0,5 um events example # 2
CLEAN ROOM ... MONITORING

It is recommended that a similar system be used for Grade B


zones although the sample frequency may be decreased. The
importance of the particle monitoring system should be
determined by the effectiveness of the segregation between the
adjacent Grade A and B zones.

The Grade B zone should be monitored at such a frequency


and with suitable sample size that changes in levels of
contamination and any system deterioration would be captured
and alarms triggered if alert limits are exceeded
The monitoring of Grade C and D areas in operation should be
performed in accordance with the principles of quality risk
management
CLEAN ROOM ... MONITORING

1 m3 sampling is NOT suitable for monitoring

The sample size ......using automated system will be a function


of the sampling rate of the instrument used.
It is not necessary for the sample volume to be same as that used
for formal classification of cleanroom and clean air devices
CLEAN ROOM ... MONITORING

In Grade A and B zones, the monitoring of the 5.0 m particle


concentration count takes on a particular significance as it is an
important diagnostic tool for early detection of failure
Comment lecturer:
Even moresoe the 0,5 um data due to the better statistical
significance

The particle limits given in the table for the at rest state
should be achieved after a short clean up period of 15-20
minutes (guidance value) in an unmanned state after
completion of operations
Clean up period 0,5 um events

At rest values after


20 Min clean up phase

13
Bad practice

!
Portable particle counters with a short length of sample
tubing should be used.because of the relatively higher rate
of precipitation of particles 5 um in remote sampling
systems with long lengths of tubing
Particle losses theoretical data

Horizontal tube
1cm inner diameter // 28,3 l/min flow

15
Particle losses theoretical data

Loss per 900 elbow


1cm inner diameter // 28,3 l/min flow // density 1 g/cm3

16
Loss of 0,5 um particles - real data - D area
Loss of 5,0 um particles - real data - D area
CLEAN ROOM.MONITORING

Clean rooms and clean air devices should be routinely


monitored in operation

and

the monitoring locations based on a formal risk analysis study


and the results obtained during the classification of
rooms and/or clean air devices
Risk analysis

Drawings in chapter risk analysis provided by


M. Hallworth/ Particle Measuring Systems Inc
Risk analysis step 1
Risk analysis step 2
CLEAN ROOM ... MONITORING

For Grade A zones, particle monitoring should be undertaken


for the full duration of critical processing, including equipment
assembly,

except

where justified by contaminants in the process that would


damage the particle counter or present a hazard, e.g. live
organisms and radiological hazards. In such cases monitoring
during routine equipment set up operations should be
undertaken prior to exposure to the risk.
CLEAN ROOM ... MONITORING

It is accepted that it may not always be possible to


demonstrate low levels of 5,0 m particles during
filling operations due to the generation of particles or
droplets from the product itself

24
Sample points as result of risk analysis
Sample points as result of risk analysis
Sample points as result of risk analysis
Sample points as result of risk analysis
Sample points as result of risk analysis

29
Alert and action limits

Appropriate alert and action limits should be set for the results
of particulate and microbiological monitoring.
If these limits are exceeded operating procedures should
prescribe corrective action

30
Alert and action limits 0,5 um

31
Alert and action limits 0,5 um

700

650

600

550

Use 2 X SD
500
or
450 3 X SD

400

350

300

250

200

150

100

50

0
1 18 35 52 69 86 103 120 137 154 171 188 205 222 239 256 273 290 307 324 341 358 375 392 409 426 443 460 477 494 511 528 545

32
Alert and action limits

For 0,5 um particle data (with good statistical significance):

A 95% confidence limit should be established for the actual events during
production.

Data can be achieved during media fills while operators are following
SOPs in normal operations.

The limits found may be less than the class limits

33
Alert and action limits 5,0 um
Alert and action limits 5,0 um

counts perr minute


5

4 Event series
#3
3

0
1 12 23 34 45 56 67 78 89 100 111 122 133 144 155 166 177 188 199 210 221 232 243 254 265 276 287 298 309 320 331 342 353
Alert and action limits

N:m = 3:10
Where t= 1 min

Drawing provided by M. Hallworth/ Particle Measuring Systems Inc

36
Alert and action limits

For 5.0 m particle data (with poor statistical significance):

A number of events per unit time should be used.


Frequency has been estimated to be no more than 3 events in
any 10 minutes to create an action (n:m = 3:10; 3rd event rule)
and potentially 2:10 events for an alert.

Values are 0 or 1 and (even though it is unusual statistics)


standard deviation is 1

One event with 3 counts will lead into an alert; one event
with 4 counts causes actions

37

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