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Report on the Results o/Assessor Responses Receiued for Exercise # 2 : Judging Compliance with the Requirements of ISO/IEC 77O25 (7999)
Intrcduction
In the spring of 2004, AZLA provided allILAC signatories and appligants with an exercise *2 that would challenge the signatories laboratory assessors to determine if the situations described in the exercise were complaint or noncompliant with the requirements of |SO,4EC 77 O25 (1.999). (ln 2002,ISRAC provided the first exercise on judging nonconformities.) Both exercises were done to determine the degree of uniformity between the assessors used by the different ILAC laboratory accreditation bodies and to allow each accreditation body to look at the results from within their own group of surveyed as-sessors.
Five situations were described in Exercise 2 Each situation contained information gathered at an assessment for which a non-conformity (NC) against the requirements of ISO/IEC 77O25 might be raised. The assessors were to exam situation carefully, and then take one of the following
l
l
:
Accreditation Body
Ema Mexico
# Assessor:
Comments
This may have been a collective response
t.lA Norway
o o
$AC.Singapore
ttdgL tnoia
SAS Switzerland JAB Japan
NATA Australia
43
tz
15
29
ZU
DMSC Thailand
17
69
1
15
a)
If they thought there was sufficient evidence to raise a NC, they would mark tl-re NC box with an X and mark the text box with the clause (or sub clause) of ISO,/IEC 17 025 against which the NC had been raised.
60
18
30
8
B
b)
If they did nof think there was sufficient evidence to raise an NC, they would mark the observation box with an X. In the text box, they would mark the relevant clause (or sub clause) of ISO,ziEC 17 025 and state iheir reasons for drawing the observation and state what further evidence they would need to seek.
DAP Germany
11
35
/o
1
,.
'i
f I
Resulfs
There did not appear to be a great deal of misunderstanding about the situations that were described for each of the
a.ssessors properly interpreted each situation. In several cases, the assessors did not carefully read the scenario and so their responses
procedure for allowing their client to monitor their own test processes, so this would be an obseruation.
were off the mark. The assessors offered an array of responses with respect to the relevant clauses of ISO,zIEC 77025 that should be cited. There was also disparity in the decisions reached between assessors concerning whether
a situaticjn resulted in a deficiency or an observation. There
The assessor could seek further evidence of compliance with clause 4.7 by observing the visiting client to see if appropriate cooperation was given by the laboratory and to see if confidentiality of other clients' work was being maintained per section 4.1.5c of ISO/IEC 17025.
7
for Scenario #
41%
Each scenario is restated below, just as it appeared in Exercise 2.Then the "expected response" (as determined by the exercise creator) is stated for each scenario. Following that is a brief summary of the types of answers that were received and specific comments if any particular trends were seen. The percentages are based on the total number of assessors that reported the required information for each scenario. This report has been submitted to the ILAC Accreditation Issues Committee for a decision on anv further actions that may be needed.
% Citing an observation
59% 56%
s.8. 5.8.1
Specific Cotntnents :
10 assessors did not give a response to this scenario.
EXERCISE # 2
Scenorio | :
At a small, privately-owned testing laboratory, the assessor noted that a client was visiting the laboratory to monitor the conduct of his testing. When the assessor questioned the laboratory's quality manager about procedures for allowing their client to monitor their own test processes, the quality manager replied that no procedures had been prepared.
10 assessors cited Note 1,A under section 4.7. Notes are not normative text.
58%
74%
Expected Response:
The assessor in this example asked the laboratory rep for a proc.edure t'or allowing their client to monitor their own test processes.
\>-
16%
49"k
4.
1
.
Specific comments:
NC
OBSERVATION
Scenario 2
Topnotch Laboratory is an in-house laboratory that supports
an automotive manufacturing company' Topnotch Laboratory's Technical Manager resigned three months
prior to the on-site assessment. Until a suitable replacement can be found, the manager of the Topnotch Production Facility has assumed the duties of the technical manager' He is ultimately responsible for the production line' the laboratory that tests samples from the production line' and the data from these tests that accompanies each production shipment. The management system documents do not
address this temporary situatton'
Many assessors cited clauses relating to the appointment of deputies. or the technical knowledge of the production
manager
47"/"
Expected ResPonse
1W" Of immediate concern is the need for the laboratory to go"/" Manager/ Technical the of define the responsibilities
conflicts
Bo"/"
7o"/"
clause
60"k
uo..^
4O"k
4.1.4.
Per
4.7.4,this relationship must be defined and the scenario 3o"k to 2o"/" states that there are no management system documents 1o"/" address this temporary situation, so this would 6e a nonconf
ormitY.
O"/"
OBSERVATION
RELAVANT CTAUSE
Scenario 3
During an assessment, a production engineer from a metals fabrication company entered its in-house laboratory and asked a laboratory technician for a microm eter. He needed to do a quick measurement of a sheet of steel to be used in the fabrication machine. He took the micrometer out to the shop floor, performed his measurement, came back into the laboratory and returned the micrometer to the technician. The technician ran a quick check of the micrometer against a couple of his gauge blocks before using the micrometer for his test measurements.
Specific Comments
6 assessors did not give a response to this scenario. Many of the assessors seemed most concerned about the production engineer's access to the laboratory. but it seems clear that because the production engineer checked in with the technician when he took and returned the micrometer, access by this production manager was not an issue for this laboratory, under these circumstances.
Expected Response
% Citinq an observation
This scenario .is allowed per section 5.5.9 of ISO/IEC 77O25, so the most relevant clause is 5.5.9.
There does not appear to be sufficient objective evidence in this scenario that a non conformity has occurred, though the assessor would mosl assuredly have to investigate further to be sure, so this is an obseruation.
4.1.5 a: 5.4.'l ; 5.5; 5.5.1 ; 5.5.2; 5.5.3; 5.5.3.3;5.5.5; 5.5.6; 5.5.10; 5.6;5.6.1 ;
5.6.3.1
The assessor should seek further evidence of compliance with the following clauses of ISO,zIEC 77025.
5.2.5 and 5.5.3, Find out if the production engineer was authorized to use the micrometer
7o%1 60%-]
50%--]
5.5.6, Find out it' the correct procedures for handling, transporting and using measuring equipment exist and were followed by the production engrneer
5.5.10: Find out if the technician's quick check of the micrometer upon its return properly followed a written
procedure.
4O"h'' 300/"-
20"/"-
10%I
O"/"
NC
OBSERVATION
RELAVAN
scenario 4
.LAUSE
73/"
48%
This commercially available testing laboratory's procedure, SOP 17.8 states in section 5 - 7:
I
I
a) b)
I I
in a blue bin. .5 a,e; 4.12; 5.2.2; 5.2.5: 5.3.4 5.4.1; 5.5; 5.5.1; 5.5.3;5.5.6; 5.6.3.1 5.8.1; 5.5.10; 5.6; 5.6.1
4.'f
Each blue bin shall be tagged with the date and time
c)
When not undergoing testing, all test items are to be slored in their bins.
Specific Comments
During the assessment of this laboratory, the assessor noticed several test items on shelves at technicians' workstations; not in their bins. When asked, a technician responded, "Well, the items are on the shelf in the order that they came in- If we don't remove them from the bins, we end up with too many bins on the floor. We remove the items in order and stack the bins. As we pull the samples off of the shelves, we know that the next sample goes with the bottom bin!" Expected response
This is first and foremost, an issue where the laboratory is not following their own procedure for handling items. because the items are not kept inblue bins when not under test; they are stored on shelves. This would be a non-conformity against the laboratory's own written procedure, SOP 17.8, sections 5-7. The most relevant section of ISOIEC 77O25 is clause 5.8.1.
The assessor would have to find further objective evidence of item confusion in order to cite against 5.8.2 or 5.8.4. As the scenario is written, there is no evidence that the laboratory's practice of keeping the items on the shelves results in any confusion.
Nearly 50% of the assessors cited either clause 5.8.2 or 5.8.4, though the scenario did not state that the assessor found any confusion in identification, or loss or damage of test items.
26"/"
\W" 90"/"
8O"/" 7O"/"
60%50"/" -
this non-conformity.
o"k _
10%
NC
OBSERVATON
*:ilXtt.
Scenario 5 The assessor at a small automotive testing laboratory noticed during an assessment that a technician measured the thickness of the wall of a tube by using a micrometer (best reading 0.01 mm). For the final judgment, the mean value of 8 separate measurements was determined. In the
test report for this measurement, the laboratory included the following statement under the "Conclusions" section of the reDort:
19%
11"/"
4.
The mean ualue of the wqll thickness of the tubes is 0.703 mm and lies aboue the required minimum
thickness ot' O.7 mm.
to calibration
Expected Response
Nearly 25o/o of the assessors cited clause 5.4.6.2 though the scenario did not give any indication one way or the
This scenario focuses around the test report issued by this laboratory. Significant figures for the final reported number
(mean value 0-703 mm) are not appropriate for the measuring device used, and so the final reported result is not accurate. Therefcire a statement of compliance cannot be made. This is a non-conformifg against clause 5.10.1 for report inaccuracy and against 5.10.3.lb for the statement of compliance in the report.
interpretations, 5.10-5, although no opinion or interpretation was provided in the report, merely a
statement of compliance.
The assessor would also need to confirm whether measurement uncertainty had been considered when
making the statement of compliance (5.10.3.1.c).
% Citing an observation
% Marking the most relevant clause. 5.1 0.1 5.10-3.1.b. 5.'l 0.3.1 c
37"/"
4.4c; 4.12:
62% 38%
or 5.10.3.1.b
.1 ;
4.4; 4.4.'l c; 4.1 0.1 ; 4.'l 2; 4.12.2; 5.2; 5.2.1 ; 5.2.2; 5.3; 5.4; 5.4.'l c;
60y"
50v" 407"
5.1 .2;
30%
2Oo/"
5.10.5
10%
O"/"
Specific Comments
Conclusions
There was a wide variety in the clauses of the ISO/IEC 17O25 standard that were cited, sometimes with little logic in the selection made by the assessors- A review of "other
clauses cited" for each scenario will bear this out.
standard. For example, section 5.8 was cited to indicate a problem with item handling, rather than the specific clause
9001, 2000 certification and ISO,zIEC 17O25: 2005 accreditation. At times the laboratories themselves have
difficulty in determining whether they need certification,
accreditation or both.
To address this problem,
on 1B'h June 2005, EO ILAC IAF (lnternational Organisation for Standardisation, International Laboratory Accreditation Corporation,
It also ",r/tas apparent that many assessors were citing nonconformity for the scenarios based on their assumptions or expectations of the cause, reason or outcome of the observed non-conformity, instead of citing the nonconformity for the situation at hand. Scenario # 4 is a good example of this. Nearly 5oo/o oI the assessors cited clause 5.8.2 because they assumed there had to be a problem with misidentification of test items, even though the scenario never mentions that.
"A laboratory's fulfillment of the requirements of ISO/IEC 17O25:2OO5 means the laboratory meets both the technical competence requirements and
management system requirements that are necessary for it to consistently deliver technically
valid test results and calibrations- The management system requirements in ISO/IEC 17025 (section 4)
the Accreditation:
1
are written in language relevant to laboratory operations and meet the principles of ISO 9OOf :2OOO Quality Management Systems Requirements and are aligned with its pertinent
requirements".
Ca'lihro,tion of aWeight
Calibration of a weight consists in assigning a mass value to the weight by comparing it againSt a reference standard of known mass whose nominal mass is equal to that of the weight under calibration
ABBAWeighing Cycle
Weight or
Pan Balance First Second
Mean
lndication
Diff.
(B_A)
Diff.
Diff.
(RA)
(B-A):
^m
This pomparison of the weights is done on a suitable weighing instrument. The indication of the weighing
instrument is used only to determine the difference between the reference standard and the test weight
A
B B
Il
l"+ L, lr+
2L,
[(lr-lr)+A B
[(r3
The comparison of two weights is always carried out according to the substitution method using ABBA or ABA weighing cycle to eliminate linear drift.
In+34
A+
[(1, -
I,) + (Ir-In)l/2
ABAWeighing Cycle
Weight on Balance Pan Indication
Frst
SubstitutionWeighing
The Reference Weight of known mass M* and the Test
Weight of unknown mass Mw are put one after another on the same weighing pan and their weighing difference Am is determined as :
Second
Mean
Dff.
(B-A)
Diff.
(B.A)
Dff.
(B-A)= Am
A
B
I1
lr+
L,
[(1, -
Ir)+
B
Al [(r2-13)-Al
[(lz
lr+
2A,
[(1, - (1,
l)
/21
Remork: 7.
2.
AB
times(n >1).
hing Cycl e
r
1. 2. 3.
A B
ABBA ABA
r.. B "A
Weig
Bl B. B3
Io,
_
B4
Ib4
Bs n Io,
aZ
86 B7 B8
Ib(
A87B2... BnA
I,
ltbr
ltbz
_
lot
Ius
Iot IA
' ,
Represents Weighing the Reference Weight Represents Weighing the Test Weight
Bt-A
Bt- A
Br-A
M* &
ABBA
& ABA are used for. calibration of E and F Class of Weights and AB1B2, ... BnA for M Class of Weights
ltbs
/2 /2 /2
: :
A-r
A-j
A-z
Weighing Equa};ion
for Detertninortion of
Mass
p*
: Mass
Reference weight
M, &
p,
P.
: Mass
Test Weight
InputQuantities
M.
VR
Volume of the Reference Weight Volume of the Test Weight Density of Air, during intercomparison
Mr (1- p^/h
) -
MR(
1- p^/pR) :
or
Am
VT
pu
Am
Weighing dif.f.erence
Output Quantities
cei
ointy
aI cul atio n s
M* : U* :
Mr:M*+ (Vr,V*).p..+Am
EXAMPIE
Suppose a 1 kg brass weight W of accuracy class F1 is calibrated against a stainless steel reference weight R of accuracy class E2 on a 1kg single pan Mettler H-315 balance with readability 0.1mg. The calculations for mass, and uncertainty associated with it are as follows, -
Input quantities
Test Weight
o'nd
their uncertainties
Density Volume
8 .4 g /cm3 ( for brass weight) dw : 1 19.047 cm3 (calculated from density dw Vw : 0.001 cm3 (assumed value with k: 2) Uvw Exp.Uncertainty of volume Standard uncertainty of Volume uu* : lJvw/ k: 0.000 5 cm3
Reference Weight
Mass
Expanded uncertainty of Mass Standard uncertainty of Mass Drift in mass of Ihe ref.erence Standard uncertainty due to drift Density Volume Expanded uncertainty of volume Standard uncertainty of Volume
Mr Ur
ur
Dr
uDr
dr
w
Uvr .uw
Mrc
Urc
ur.
0.000 006 g 7'9 g /cms : 126.580 cm3 : 0.000 5 cm3, k:2 -- lJvr/ k: 0.000 25 cm3 : 999.997 63 s 0.000 03 g : Urck: 0.000 015 g
Dr
:999.999 53
(from calibration certif icate) (from calibration certif icate) (from previous data)
( negligible)
(from calibration certif icate) (calculated from density dr ) ( from calibration certificate) (from calibration certificate) (from calibration certif icate)
Sensitit:ityWeight
TYPE B
Mass
Standarduncertainty
r.
5.008 mg
(i)
: :
Air Density
Measuring temperature, pressure and relative humidity of air, the air density is calculated using BIPM Formula or air density table. Thus air density and uncertainty in its measurement may also be treated as input quantities.
0.000 045 g
0.00000fu
u(m,)
: 0.045 mg
(ii) ub2
: 24.4oC ; Pressure : 7 4I.25 mm Hg; : 560/o : 0.001 116 g/cms Air Density pu Standard Uncertainty Upu : 0.000 05 g/cm3
Temperature Rel. Humidity
pa
( u u*2
- u,,2) .pu2.
.( 0.00005g,/cm3)2
(O.O
: :
+[ ( 0.00o5crn3)2 {0.00025crns) ? x
OttL@/cnt\2
Measurement Dsta
Mr - Mw: -2.10 Mr - Mw : -1.95 Mr - Mw: -2.10
Iklecln : -2.O5 mg
Am
O.O9mg
n:3
(a)
due to display resolution. Other components i.e. uncertainty due to eccentric loading and due to
magnetism, will be negligible.
2.05 mg
Moss of
Mass Mw of the test weight W is given by the weighing equation (1) as follows.-
:
(b)
u
Mw : :
Mr + pu (Vw- Vr) + Am
(d
'16,i
0.1
/'16:
o.o+r mg
g + 0.002 05g
uu": {(
u.2 + u62)
0.041 mg
Totol Type
(0.0a1mg)?
'uA
/ ',1 n:
0.09
/ 'l 3 :0.052
mg
10
'\L
nty
Final Results
:
:
: J( uoz + uu2 ) :
r/ t (O.OSZmg)2+(0-355 mg)2 I
0.36
mg
Expanded UncertaintY
Mw = ( ggg-993 77 t O'OOO 72 ) s, k
:2
kxu.:
2xo'36mg
o'72mg
Reference ueight,
Mass
Normal
Rectangular
Drift in mass
Buoyancy Correction Bo,lo'nce: Sensitivity Display resolution
Normal
Rectangular
Totrrl Type B
Co mb in ed st an
dard
un
cert
ainty
u"a
(m)
v"fI : h-
7)
2 x (0.36)a / (O.O52\4
:
2x2297
: 4s94
u-a (Lm)
Forv"r, : *
Expanded Uncertainty
k:2 U
2xO.36 mg
O.72 mg
Drift in mass of lhe reletence Density of the reference weight Density of the test weight
Mr: ( 99.999 86 t 0.000 02 ) s,k:2 (from Previous data) Dr : 0.000 01 g dr. : ( 3040 t 16) kg/mz ; k:2 dw = (7900140)kg/m3 ;k:2
t1
Obseruations Dqtcr.:
- Mr - Mr - Mr Mw- Mr Mw- Mr
Mw Mw Mw
V,: 0.100 ks/BO4Okg/^3: 0.000 O72Mm3:72.M V*: 0.100 ksngoo kgl-3: 0.000 O72 66 m3 :12.66
cm3
cm3
M.:M, 1(V*-V,).pu+Am
:9.999 86 g + (72.66 -L2.441cm3x 0.001 160glcm3
0.000 09 g
99.999 86
g + 0.000 255 g
+ 0.000 09 g
t)
rd
:001
Deuio,tions Sguares 0.00 mg 0.0000 - 0.01 mg 0.0001 - 0.01 mg 0.0001 0.00 mg 0.0000 +0.02 mg 0.0004
0.0000 ms
0.0006
mg
0.09
Mean: 0.09
Standard Deviation, o
p" :
[0.
tt ]/( 27 3.I5+t)
: :
(273.I5 + 22.5
0.001 160 g /
cm3
: L2.44 x 0.001 : O.Ot2 S crn3 dr : (79OO t 40 )kg/ms , udr: @O /k)kg / m3 : 20 kg / nts (k :21 (uo*/ d,: uvr / Vr ) or (20 /T7OO : ,vt 12.66) /
uv,
buoyanay correction
or(0.0025:uvr/12.66) uv. :72.66 x 0.002 5: O.OS7 6 cm7 Standcrd uncertainfy ossocic ted with the air
us:
u.:
\tqf
{(uo2 + uu2)
O'O39
IJ
^g
ncertainty
,b2
: :
r u*, -
:(n- 7) :
14806
u.a (mr)
u,,4 (Ltn)
uu,2) eoz
(1.160 mg
/ un :
cm3)2
Expanded Uncertainty
:-
0.001351
O'O37
U:
kXU.
: 2x 0.039 m9 :
)g
O.Og mg
^g
Final Resulfs
Uncertaintg Budget
Probability distribution
Weighing process coeff icient uncertainty mg
O.OO5 mg Normal Rectangular
Sensitiuity Stqndard
Reference weight:
Mass
Drift in mass
Buoyancy Correction Display resolution
Total Type B
Combined stan dard uncertainty
Y
"ff
= (n-I) x
For
y
u.a (mr)
u,u4
(Lm)
4x(0.039)4
"ff
: k :2
2 x 0.039
Expanded Uncertainty
mg
O.O8 mg
13
7. Introduction
This paper describes general procedure for the calibration and the uncertainty of calibration of a weighing instruments used in a calibration laboratory for calibration of weights. An attempt has been made to arrive at an uncertainty which can be associated with the results of practical weighing. This is the uncertainty of weighing.
provided to set the weighing range, then this should also be provided, even if it is outside the limited weighing range as defined above.
The '"yeighing instruments considered here are nonautomatic, single interval instruments which include
balances and electronic apd mechanical industrial weighing
equipment.
Their buoyancy in the air in which they are used affects the apparent mass of weights used and this changes with the air density. The calibration value of the weights needs to be certified for air density 1.2 kg m 3. If the buoyancy effect caused by a different air density at the time of use leads to an error in the applied load that is greater than one half of the resolution of the weighing machine being calibrated, a correction should be madeWeighing machines as described in Table
The test procedures used in the calibration are based on those given in OIML Recommendation R76-7 and that for the evaluation of uncertainty is based from the Guide to the Expression of Uncertainty to Measurement (GUM).
can usually be
specifications. The table assumes that the uncertainty of calibration of the weights used will be l/3 of its specified maximum permissible error. In most cases it will be possible to obtain smaller calibration uncertainties than this, and it may therefore be possible to use a weight of a lower class. However, when selecting suitable weights, attention should still be given to properties of the weights other than accuracy, such as magnetism, corrosion and wear resistance. In most laboratory applications, it would not be apprcpriate to select a class lower than M1.
Resolution g
7os
M3 M3 M3 M3 M3 M3 M3
M1 F2
7g
M3
7OO mg M3 M3 M2
M1
F2 F1
7O mg M2
M1 F2
F1
7mg
F2
F1
O.7 mg
E2
E1
<O.7 mg
E1 E1
Upto50g
Up to 100 g Up to 500 g
M3
Uptolkg
Upto5kg
Up to 10 kg Up to 50 kg Up to 100 kg Up.to 500 kg
M3 M3 M3 M3 M3 M3 M2
M3 M3 M3 M2 M1
F2 F1
E2
E1
E2
E1
E2
E2
t4
g[r
3.
Calibration Procedure
The documented procedure for calibration of a weighing machine should include sufficient measurements to define the performance of that
machine-
of readings. It is not necessary for the weight used for a repeatability test to be traceably calibrated-
it may happen that same value of the differences may be obtained for all repeated
Some times measurements. In that case standard deviation will be zero.lt can be shown that if one of the n readings depart from zero by dx then the standard deviation is given by
If the machine to be calibrated is a electronic, it has 'internal calibration' facility that allows the output of the machine to be adjusted between zero and an internally or externally applied weight, in that case it is necessary to operate this facility prior to the calibration, and also it should be operated regularly before the weighing machine is used.
For the balances having electronic display, sometimes
= l/3(readability
Therefore to be realistic, the minimum standard deviation of a balance should be one-third of its
readability.
Maxrl/2.
All weighings involve a minimum of h,vo readings, a zero reading and a reading with a weight to be measured- If this difference is measured a number of times it is a good measure of the repeatability of the reading. Usually a minimum of ten repeated
measurements are taken when calibrating weights up
used across its range, it would be appropriate to measure the sensitivity with no load, loaded at half its capacity and loaded at or near its full capacity. For electronic balance with digital display the idea of sensitivitgr needs to be modified slightly. The electronic
errors may cause the balance indication to depart from nominal value. So rather than refer to sensitivifu
15
it is preferable to
say departure of
indication from
2. 3.
Remove the weights in reverse order, noting the balance reading after each removal
Compare the readings for the same load being applied
(c)
Significant deviation between the increasing and decreasing readings indicates a poorly adjusted or dirty balance The laboratory should set the error allowed for a particular machine, for a particular test, after considering the use to which the rnachine is put. Manufacturer's specifications for weighing machines will often be inappropriate for the application.
in error between points. Usually this covers at least 10 points, evenly spread over the range. For 'machines that have internal weights (e.g. dial-up weights) each weight setting should be tested. For machines having more than one range, this test
should be carried out for each range used.
In order to comply with the requirements of ISO,/IEC 77O25, the laboratory needs to ensure that a suitable
uncertainty of measurement is calculated for the weighing machine calibration.
It is not necessary for the weight used for the eccentric-load indication test to be traceably
calibrated.
7- Repeatability ( Tvpe A)
Repeatability of a balance is usually determined by making 10 measurements at particular points across
the range of the balance and then calculating standard
(f) Hysteresis
Hysteresis is occurring when a balance, for the application of the same weight, displays a different
reading when the load is ascending compared to when
deviation (s) of these 10 repeated measurement results. This is Type A uncertaint5l and is given by :
uo
s,/
{n, n:10
2.
each
component in uncertainty of the balance. It is given in the calibration certificate of the reference weight. Thus standard uncertainty due Io reference weight is
Or
u*:U*/k
3.
Resolution of the bo'lo'nce (Type B)
Resolution limitations in reading
u,",, :
6.
'
the
scale or with a.
uo:
(d
/2.'B)x^12
and zeroi.
it
is
8.
Combineduncertainty
Total Type B uncertainty ue
Combined uncertainty u.
: {[ uo2 +
u^
an amount approaching the uncertainty. If this drift is Dr then assuming rectangular distribution, uncertainty due to this drift is
uD,ift
9. kpanded uncertainty U: k.
E}{AMPIE
Dr
5. Drift in Sensitiuity
fron
Temperature effects on the scale sensitivity of the balance. We need either the actual change in scale sensitivity between the beginning and end of a calibration or we assume the coefficient relating scale
sensitivity drift to temperature. The two possibilities
Capacity : 2lO g
Readability
0.1 mg
2 ppm/"C
7. Repeatability ( Type A)
Choosing
are
u."..
p:
maxva\re/N3
t7
Measurements
1
Indications (I)
(g)
Deviation (di)
(mg)
d12
100 000 0
2
J
100.000
+ O.02 + 0. 12 + 0.02
0. 08
0.000 4
0.0r4
4
5
6
.7
100 000 0
8 9 10
99 999 9 99.999
B
018
+ 0.02 Sum
092 mg
100.000 0
Mean
Standard Deviation
99.999 9a
0.000 00
Sum
0.076 0
s: vlo.ozo 0 / 9):0.
:
5. Drift in Sensitivity
un: s,/!n
2.
:0.092/.,1 70:0.029mg,
Given drift in balance indication with temperature as 2 ppm/"C. For 1009 mass the coefficient relating scale sensitivity drift to temperature
un
/ 2:
0.000 010 g
0.010 mg
ua =
0.10046/
{3
mg
0.0
/2
^B ) x'12
=
6
Combined uncertainty
4- 'Uncertainty
(0.072)21
If Dr = 0.000 015 g from the previous data then uo,ift: 0.000 075/2\13 : 0.0075/ {3mg : 0.004 mg
U:2x0.078g=0.16mg
-"l
Uncertainty Budget
Typ.
A
B
Source
Repeatability
Mass of the reference
VaIue mg 0,o29
0.020
Probability distribution
Normal Normal
Dioisor
1
Degree of freedom
9
@
I
1
weight
B B B
Drift in mass
Display resolution Sensitivity variation
0.0075
0.071
./ s
I I I
'^/
^/
s s
0.1005
up,,112
Totc.l Type
B :
^/
(u^' * ,o2 *
,,n,,.2
o.o72
o.o78
9 x(0.O72)s
"ff
: (n-7) x
u.4 (mt)
u-a (Lm)
(O.OZg)a
: 9x38 : 342
For tt"ff :
: k :2
U:2x0.078mg:0.16mg
Expanded Uncertainty
,
I 1
o
Er ' .
after weighing (T2) is measured. Mean of these two temperature is the temperature of the water (Tw).
The mass of water (Mw) contained in the measure up to the mark is calculated using following relation: Mw
Set-up the balance in weighing condition and select suitable standard weights, necessary for this calibration work.
( 7-
p"/
p*)
r .r, . Thevolumeofwater,VmatthetemperatureTwisgivenby; { ,,rI., -----....--.-t^ and a standard weight ot Wciigh the empty measure mass Wl (approximately equal to the mass of distilled Vm : Mw / p* -- ( 1- p^/p,). ( W1 - W2)/(p* - p^) ti" \ water of nominal volume of the measure) The voiume Vm at th treference temperature 27"Cis given@;
Weigh the measure fully filled-up with distilled water some required standard weights of mass W2
ure of distilled water before weighing (T1)
Vzt : Vm / 11*
0(
I* - 27 )l
and
t9
UNCERTAINTY CALCULATIONS
MEASUREMENTS
IN
VOLUME
of
The contribution factors in the uncertainty of the estimated value of the volume of the measure is mainlv due to two
sources of errors
,
R.H :
Temperature of water Initial
986 mbar
48.6
o/o
1. 2.
(.I2)
22.4oC
g
-- 0.gg7 6932
/,
Unce.rtqinty due to Weighing Process ( Type A ) The uncertainty in the weighing process is due to the
variability of the balance which is generally obtained from the past history of the balance using the same method of weighing as used in this calibration procedure. Suppose pre-established standard deviation of the balance using this method of weighing is s then type A standard uncertainty is given by :
Readability
un: o/!n
where n is the number of observations taken to estimate o.
: e\.OI t
0.01) m g : k
: 2
certificate
Mass of the empty vessel + standard weight
coverage factor
k:2,
obtained from the calibration certificate of the standards, then standard uncertainty due to the standard weight will be ,
Mass of the empty vessel + distilled water+ standard weight (w2) 150 002 86 g
u":Us/k,
Uncertainty due to other contribution factors such as densities of the air . of the water and that of the material of the standard weigh are very small and may be assumed to be negligible.
Total type B standard uncertainty will be U-
W1
50.000 019,
W2:
O.O25
(W1-W2) + (R2 - R1 )
49.976 34 g
8.000
cms
:
*
u..
T
)
: 22.35"C p :
1uo2"
ur2
Vm
EXAMPLE
= ( 1-0. 00
of a
0.99985437 5 x 49 x
6 Y/O.9965282
: 50. 7 43 7 5 qns
vzt:
20
Vzz:
UNC
5O.743 27
cm3
0.9999163
SO.7J7 cms
/ n:
.'l
O.02 mg/.110
0.006 mg
U :k. v : 2x 0.0306*s: 0.0612mg : O.O6L2/ 0.997 6932 cm3 U: r O.O67cms Stqndard Uncertainty Type B ( due to display resolutiori) Final Resuffs Volume of the Volumetric Flask ud - @/2 {3 ) x ./Z (a : 0.01 mg) : (50.137 t 0.061) cm3, k:2 = 0.004 mg Uncertainty Budget
Type
Stqndqrd Uncertainty Type B ( due to stbndard used) Us : (0.05 + 0.01) mg : 0.06 ms ; k :2 then uB :u, : 0.06 mS/ 2 : 0.03mg
uncertainty
Sources
Due to Weighing Process
Estimated Sfandards
Uncertainty
Type A
Degree of freedom
us
O.OO6 mg
Type B
ut
2mg
O.O3O mg
0.025 mg
u"2=Usullk :O.07/2
mg
0.005 mg
Type B
ubo
d:
Total Type B
O.OO4
mg
0.01 mg
O.O3O mg
ua2
) = O.OSO 6 ^g
9x(0.0306)n
/(o.ooolo
6089
: *
cm3
0.061 cm3
2l
3. A wooden
rectangular board slightly wider than the width of the jar, whose top half is painted black and bottom half white. The line separating the black and
known.
The hydrometers to be calibrated is floated in a liquid of appropriate density which is so adjusted that the level of the liquid surface intersects the scale graduation under examination. A similar standard hydrometer is floated alongside and indication of its scale is observed carefully. Differences between the scale reading of the standard and under test hydrometer gives the correction to be applied in the scale reading of the under test hydrometer to get its actual value of the scale reading.
white portion is horizontal. The screen is movable about its horizontal axis and it is placed behind the jar at an angle of 45o in such a way that line separating black and white portion is just below the
liquid surface. This screen helps in keeping the correct
line of sight.
thermometer graduated in 0.1oC with a calibration certificate of scale correction is used to measure the temperature of the ref,erence liquid. A thermometer oI range - 0.5 oC to 40.5 oC is suitable for this purpose.
5.
jar, with its front and back walls being parallel. The front wall is made of optical glass, which is plain and polished from outside. This prevents the distortion of the image of the scale of the hydrometer. Except for abnormal hydrometer a jar of about 112 mm length, 62 mm width and 360 mm height will be suitable to accommodate two hvdrometers with stirrer and a thermometer..
The hydrometer vessel set-up is installed in a closed chamber equipped with exhaust system to suck out fumes of the liquid used. Because of the toxic nature of the liquids, the atmospheric conditions are kept reasonably vapour free using an exhaust system which draws the vapour downwards, thus taking advantage of their high
density.
6.
2.
A stirrer is used to stir thoroughly the reference liquid in the jar so that air may not be entrapped in the liquid. The design of the stirrer is of the special type having perforated rectangular metal sheet whose dimensions are 2 mm less than the those of the cross section of the jar. A stout rod is screwed in the center of the metal sheet and works as handle.
The hydrometers are calibrated under normal room temperature conditions. Appropriate corrections are applied for hydrometers graduated for density or relative density at reference temperatures. These reference temperatures are generally 20 oC, 15 oC, 15.5 oC or
that desired by the users.
The calibration is done in the following steps:
1.
22
2.
Allow the liquid to attain thermal equilibrium with its surrounding and then pour it into the hydrometer vessel fiar). Avoid the formation of air bubbles in the liquid by pouring it down the side of the vessel. Stir the liquid vertically with the stirrer, again avoiding formation of air bubbles. Record the temperature of the liquid nearest Lo O.2o C.
Insert the hydrometer to be calibrated, carefully, into the liquid holding it by the top of its stem. Release the'hydrometer when it is approximately in its state of equilibrium. Adjust it so that the liquid surface level intersects the scale graduation to be calibrated.
8
horizontal liquid surace and the stem. When taking the reading, view the scale through liquid, adjusting the line of sight so that it is in the plane of the liquid
surface.
If the liquid is opaque, record the reading where the meniscus merges into the stem of the hydrometer
Immediately after taking the reading as in step 6 or 7 measure the temperature of the liquid to the nearest O.2o C. The mean of this temperature and the initial
temperature referred in step 2 should be used to calculate the correction due to temperature, if required.
When the hydrometer is in steady state, press the top of the stem downwards a few millimeters beyond the position of equilibrium. Withdraw the hand and observe the meniscus as the hydrometer oscillates to equilibrium. If the stem and the liquid surface are clean, the meniscus shape will remain unchanged as the hydrometer rises and falls. If the meniscus shape changes e.g. if it wrinkles or distorted by the motion of the hydrometer, lack of cleanliness is indicated. In
such case the hydrometer and vessel should be cleaned
The difference between the initial temperature and the final temperature should not exceed 1 oC and if
a larger difference is found, it indicates lack of thermal
Repeat steps 5 to B using the second reference standard hydrometer at the same graduation point.
10.
are
A.
Certif icate correct ions: Certificate corrections of the reference hydrometers are taken from their
calibration certificates and are added algebraically to the scale reading of the hydrometer under test, at that particular point.
When the two hydrometers which must not be touching each other and the side of the vessel, have
settled down to their equilibrium positions, record the
scale readings of both
If the liquid is transparent the scale reading is taken corresponding to the plane of the intersection of the
Tetnperature Correction If the two hydrometers under comparison do not have the same reference temperatures then their indications will differ by an amount proportional to changes in their volumes caused by thermal expansion of one with reference
23
IE
to the other. In such cases a temperature correction, as given below, is applied to the indication of the reference hydrometer to get the actual measurement
results ,
-
Tr:
surface tension of
c :
Where c :
R.a (t.-t)
(1)
correction to be applied to the scale reading of the reference hydrometer in g ,/ cm3. density indication in g
R:
cm3
a : t. : t :
If the hydrometer under test has Tu as its surface tension while standard hydrometer was calibrated for surface
tension Ts and if the two are compared in a liquid of surface
tension
Forglassa :
25x\O4 /oC,
then
(2)
c : 0.000025R (t"-t)
C. Surface Tension cortection:
If a hydrometer is used in a liquid whose surface tension is different from the one for which the hydrometer has been calibrated, then a correction called surface tension correction has to be applied to the observed scale reading to get the correct indication. This correction is given by :
of the horizontal liquid surface, a correction called meniscus correction (MC) has to be applied- This correction is given bY :-
C:
1000.i.o
I!
(1 + 2.g.d2.p0,21000o)-11
( S ,/ cm3
1
"
'(4)
o : d :
po
c : [rc.R d (T -
T1)
X 10 3l / k.ml
3.
.... (3)
Where
c:
R
3)
: : :
density indication in g/cm3. stem diameter of the hydrometer in mm acceleration due to gravity ( m/s1
surface tension of the liquid used (mN ,/m).
s : g :
d g T
(m / s2l
24
For ready reference, the values of MC in kg/m3 have been tabulated below for various series of density hydrometers conforming to BS 778 : 1979.
The scale lengths are given in third row and surface tension in column 2 in units of mN/m.
Table
L20
L50 and
L5OSP
s50
55OSP
o-2
tt3 t27
7B 99
87 702
50 62
50 62
Surface
The values f
MC inkg/m3
2.O 2.O 2.O
tenson
15
o.32 0.28 0.36 0.32 o.36 0.32 o.44 0.40 0.48 0.44 o.32 0.28 0.36 0.32
0.8 0.7
0.8 o.7 0.8 0.7 0.0 0.8
1.0 0.9
r.2
1.0
1.8
r.6
25 35 55 75
2.4
2.O 1.6
2.4 2.O
2.2 t.6
L.61.2
2.8 2.4
1.8
1.4
3.2
2.8
1500
35 55
75
3.0 1.6
2.4 2.O 2.8 2.4 1.0 1.6
0.40 0.36
o.32 0.28
L.4
7.2
2.4
2.O
2000
55 75
0.0 1.0
2.O 1.6
0.36 0.32
0.8 0.7
r.2 t.o
2.4
2.O
2.41.6
25
For routine calibration, contributions in the uncertaintgr from the other factors such as corrections due to temperature or surface tension or the meniscus corrections may be assumed to be negligible- But for high precision measurements contributions from these factors are taken into accounl and are estimated as follows,
(Type B)
If temperature correction is applicable and it is say
TC then
u*,/ {3
(1)
where u* is an estimate of minimum variation equal to either half of the observed variation width or the scale interval d of the graduations of the hydrometer scale,
whichever is greater.
urc: TC/bB
cortection ( Type B)
.....(3)
is
The half of the difference between the two measuremenr results using two standard hydrometers gives-the value of u* from which uo is calculated using equation (1) above.
rbrc:
STC/2.1
(4)
MC
/ 2'l 3
.(5)
uB: us:Us/k
Since the reported value of the hydrometer is the mean of the two observed values from the two standard hydrometers, the Type B standard uncertainty due to
standard will be
:{
[(u,)2
+ (ur.)2 +
(urr.)' + (u"6)2 I
...(6)
./ [(rn)2 + (uJz
.....(71
uncertainty U : k. u"
.......
(B)
ue
{[( u.r2 +
u,22
)/
4l
(21
26
EXAMPLE
Reference temperature(RT)
Surface Tension
27oC
Calibration of a density hydrometer having same reference temperature(RT) and surface tension (ST) as that of the standard hydrometer and liquid employed is also of surface tension equal to the reference surface tension.
(fu) : 35 mN/m
Range
0.000
g/cm3
Range
Scale interval
: (d) :
0.000 5 g/cm3
'
35 mN/m
Table 2
O bser o ations an
d Colc ul o'tions
Rounded
(Unitsin S/cm3)
Stando,rd I.D-No. Obserued ScoIe P.eading
Corrected Scole point Calculated NIean oalue of the correction Correction Under Test 4
0.700 10
I
S1 S2
2
0.700 22
I
.000 11
o.7od rs
0.720
SI
S2
S1
t+
+0.000 02
- 0.000 12
+0.000 16 0.720
0.000 14 0.000 15 0.000 2
+0.000 14
+0.000 06 +0.000 06
- 0.000 04
l0
o.740
+0.000 10
+0.000 08 - 0.000 02 0.750 - 0.000 06
- 0.000 04
S2
S1
0.000 09
0.000
S2
- 0.000 0
27
Table 3
Calculation oJ uncertainty due to nreasurement Process (Type A )
(Unitsin g/crn3)
Scale points
Obseroed
uo
uaricjion width s2
a* w
(a., /',1 31
SI
0.700
o.720
+0.000 12 +0.000 14
+0.000 08
- 0.000 06
o.740 0.750
- 0.000 02
value.
a* is taken as d : 0.000 5 g /
cm3
Expanded uncertaintV U
k. u.
u:o.ooo6g/cm3
2 x O.O0O 3
g/
EXAMPLE 2
Calibration of a density hydrometer having different
reference temperature(RT) but same surface tension (ST) as that of liquid employed Then the certificate correction and temperature corrections using eq(2) will be needed to apply to the indications of the standard hydrometer.
ue:O-OOO29g/"^3
Uncertaintg due to Standsrds ( TVpe B)
The expanded uncertainty of the standards used to calibrate the hydrometer from its calibration certificate is
with k
:2,for :
Us
each hydrometer.
u,l :
u,2
(0.850 to 0.900) s
cm3l
Since the reported value of the hydrometer is the mean of the hvo observed values from the two standard hydrometers, the Type B standard uncertainty due to standard will be
1)2 + (0.000
Il2l/4
:
: :
0.000 O7 g / cm3
: '
0.000 1g
35 mN/m
cm3
(RT): 20 oC
Surface Tension
(Ts)
28
Table 4
O bser u at
Stando'rd Observed
Corrected
Correction
lD.No.
7
ScaIe Reo,ding;
2
0.850 46 0.850 38 0.870 24 0.870 58 0.890 84 0.890 26 0.900 74 o.900 22
CC
3
0.000 04 TC 0.000 15 CC 0.000 08 TC 0.000 15 CC + 0.000 06 TC - 0.000 15 cc - 0.000 10 TC - 0.000 15 CC 0.000 10 TC 0.000 15 CC 0.000 04 TC 0.000 15 CC + 0.000 08 TC - 0.000 15 cc - 0.000 04 TC - 0.000 15
S1
4 o.850 27
0.850 15 0.870 15
Rounded
a
+ o.ooo 2
0.850
+ 0.00021
s2
s1'
+0.000 15 +0.000 15
0.870
+ o.ooo 24
+ O.OOO 2
s2
S1
S2
S1
s2
(Unitsin g/cms)
Scale points
0.850 0.870 0.890
UA
Q-
SI
+o.ooo 27 +0.000 15 +0.000 59
s2
+0.000 15 +0.000 33 +0-000 07 0.000 12
0.000 18
0.000 52
0.900 + 0.000 67 + 0.000 03 0.000 64 0.000 5' 0.000 29 : As.half of the observed variation width is less than d value, a* is taken as d : 0.000 5 g / cm3
29
7lF
Us
:2
Sbndard uncertainty
u.r:uo:Us/k:0.000 2/2:O.W
g/.
Since the reported value of the hydrometer is the mean of the two observed values from the two standard hydrometers,
of stem of both the hydrometer and calculate surface tension factor (STF) for each and apply the correction
separately to the indications of the each hydrometer using formula STFu (T-Tu) and STFs (T-Ts). But normally T:Ts then the correction applicable is only to hydrometer under
test.
u,: {[ ( u,r, *
u,22
)/ 4 I :
0.000 07 g/cm3
Also lactometer reading is taken at level liquid surface observing through liquid. But lactometer when used in milk observed at the level where meniscus meets the stem, so
meniscus correction is also to be applied to the lactometer.
4,
0'000 75 g/cm3'
Assuming rectangular distribution standard uncertaintv due
For Lactometer
Range
Scale interval
is
: :
0.000 75 / 2./
(d)
' 50 rnN,/m STFu lcatcututed from irs mss and Stem Dia.) .. 0.000
For Density Hydrometer
Surface Tension
(-fu)
O34 s2TsrnS
Combined uncertainty:
Combined uncertainty u.
Range
(
:{
={
uo2 +
Scale interval
uu2 ) 0S)21
: 0.000
g/cm3
(0.00029)2 + (0.000
0.000 30 g/cm3
: 35 mN/m
mN,/m
Assuming
T:
Ts
Expanded uncertainty
The expanded uncertainty U
: :
k.u"
2 x 0.000 3Oglcm:
sp gr.: (Corrected Indicated density/Density of water)(both densities are in the same units and at same reference
temperature)
0.000 6 g/cm3
Density of water at 27oC
:0.996
5155g,/ cm3
30
Obseroations Sheet
Standard
l.D.No.
Table 6
Observed
Scale
Correction
g/cm3
Corrected value
g/cm3 0.996 26 g/cm3 (0.999 74) sp.gr 0.995 42 g/cm3 (0.998 90) sp.gr
1
Reading;
S1
Calculated
Mean
correction sp.gr
+ 0.00'1 00
Correction
Rounded
CC +0.000 06 TC - 0.000 30
GC - 0.000 08
sp.gr
1.000
sp.gr
+ 0.000 58
sp.gr
+ 0.000 6
S2
S1
sTc - 0.000
MG
51
.015 92 g/cm3
S2
S1
cc
S2
S1
S2
cc - 0.000 12
TC - 0.000 30
- 0.000 75 0.998 74 1.020 sTc - 0.000 51 MC - 0.000 75 1-O18 74 1.029 05 sTC - 0.000 51 MC - 0.000 75 1.028 74 1.940 sTC - 0.000 51 MC - 0.000 75 1.038 74
+ 0.000 16
+ 0.000 73
+ 0.000 41
+ 0.000 09
+ 0.000 4
- 0.000 4
+ 0.000 29
+ 0.000
0.000 14
Table 7
Calculation of uncertainty due to measurement Process (Type A (Units in sp.gr)
)
Scale points
Obseroed oo,riqtion
UA
Q-
width
1a- /,,1 3)
SI
1.000
s2
+0.000 16 +0.000 09
- 0.000 78 - 0.000 14
+0.001 00 +0.000 73
- 0.000 10
0.001 .
t.o20
1.030 1.040
+ o.ooo 72
'
than
d value, a* is taken as
0.001 sp.gr
31
Combined uncertainty:
u.: v(uo2 *
0.000 65
ue2)
:{t(0.00058)2 +
(0.00029)21
g/c z
i.e.
u,
0.000 07 g / cms
Expanded uncertainty
= k.u.
2 x 0.000 65
g/c
= 0.001 3 g/cm3
{.00030g/crn3
Assuming rectangular distribution standard uncertainty due
CORRIGENDUM
is
- Bangalore contributed
0.000 30
/ 2v3 :
cm3'
-0.0005l g/c
the
z'
usrc:
(Type B)
0.000
the
meniscus correction is
-0.00075 9/cm3'
Assuming rectangular distribution standard uncertainty due to meniscus correction is
uMC
0.000 75
cm3'
All assessments to take place on the basis of ISO/ IEC 17025:2005 from Januarv 0t. 2006.
All accredited/ applicant laboratories under going assessment after January 01, 2006 to submit revised Quality Manual as per ISO/ IEC 17025 2005 (if required) atleast one month before the date of assessment.
ue={(u.2+u,"2 + urra2 +
./(o.ooo o7l2 + (0.000 09)2 + (0.000
iii)
0.00029g/cms'
32
Ptogranntne Progrannme
Porrimeterc
code
TM
Nodc,l
labratory
Technologists,
Last
n(nne
Metallographic Testing of Steel
Subodh
Datefor
Registration
30.10.2005
(Group A, B, C, D
lE
Mumbai
TC39
The request for participation in the above programme rnantioning the ptogramx7,e code number DD fot the requisite o,mount may be forwarded lortest by the date as giuen aboue-
and enclosing
Five more proficiency testing programmes on Electrical and Electronics testing which were launched earlier are still open for participation. The interested laboratories may participate in these programmes. Please refer to our website www.nabl-india.org for details-
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Note:
For information on new proficiency testing programmes, NABL is reaching its accredited/applicant laboratories as well as other users of NABL services by direct communication, NABL News and NABL website- All the interested parties are requested to keep themselves abreast of the information available in relevant media.
i-
rsolEc
17025.
This is a four-day residential training programme and the course fees is Rs 7,000,/- per participant.
N ABL Assessors
Training Course
National Accreditation Board for Testing and Calibration Laboratories is seeking individuals with technical knowledge
and current experience of working in a laboratory to train them as its technical assessors to conduct on- site assessments
The numbers of seats for each training programme are limited- The selection of participants is at NABL's discretion.
Training Schedule
S. No.
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*hedule
OcI24-28,
2OOS
Coutse
NABL Assessor Course
Temperature Calibration Laboratory Quality System Management and Internal Audit Course
2 3.
4 5.
6.
7.
Laboratory Quality System Management and Internal Audit Course Length Calibration
Pressure and Vacuum Calibration
NPL. New Delhi NPL, New Delhi NITS, BIS, Noida NITS, BIS, Noida
NABL Assessor Course Laboratory Quality System Management and Internal Audit Course
8.
34
Conto.ct Details:
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EKIUltrl), Mutnbai
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& calibration
laboratories and be
Mn M.VN. Nloho,n, National Accreditation Board for Testing & Calibration Laboratories, B-4, Aparhnent, Qutab Hotel New Mehrauli Road, New Delhi - 110016 Phone: O7l- 26529718- 20,26526864 Fax: 011- 265297 L6 E-mail : training@nabl-india.org (For updated informo,tion on schedules of NABL training courses, you are requested to uisit NABL ue,bs ite.: www. no,bl-indio'. org)
35
Testing Laborstories
S. No.
1_
2. 3.
4. 5. 6.
t.
8. 9. 10. 11.
t2.
13.
74.
15. L6.
L7.
18. 19.
20.
27. 22. 23. 24. 25. 26. 27.
28.
29. 30. 31. 32. 33.
34.
35.
I-o,boroltoryNo'me Aglow Quality Control Laboratory Pvt. Limited, Kolkata Aquadiagnostics Water Research & Technology Centre, Bangalore Bhagavathi Ana Labs Limited, Hyderabad Central Forensic Science Laboratory, Chandigarh Central Institute of Hand Tools, Jalandhar Central Materials and Processes Laboratory, Foundry & Forge Division, HAL (Bangalore Complex), Bangalore CTR Electronics Test Laboratory, Aurangabad Electronics Test & Development Centre, Chennai Hindustan Coca-Cola Beverages Pvt. Ltd, Ameenpur Independent Testing Laboratories, National Council Tor Cement & Building Materials, Hyderabad Laboratory of Government Examiner of Questioned Documents, Hyderabad Laboratory Services Division, Sargam Metals Private Ltd., Chennai Manisha Analytical Laboratories Private Limited, Mumbai Metal Testing Centre, Chennai Metallurgical Laboratory, Heavy Vehicles Factory, Avadi, Chennai Micro Engineering and Testing Laboratory, Rai, Sonepat Network Clothing Company (P) Limited - Testing Services (NTS), Tirupur PhysiChem Material Testing Laboratory, Nashik Pollution and Project Consultants, Kolkata Quality Assurance Laboratory, GAIL (lndia) Limited, Lakwa Quality Assurance Laboratory, Raymond Limited Denim Division, Yavatmal (Maharashtra) Quality Control Department, Kochi Refineries Limited, Ambalamugal, Kerala Quality Control Laboratories, Birla Cement Works, Chittorgarh (Rajasthan) Quality Control Laboratories, Chanderia Cement Works, Chittorgarh (Rajasthan) Quality Control Laboratory for Processed Foods, Ludhiana Quality Control Laboratory, UltraTech Cement Limited. A.P. Cement Works, Tadipatri Regional Laboratory, Textile Committee, Ludhiana Reliable Testing Services, Mumbai Scientific Services, Tata Steel Limited, Jamshedpur SGS India Private Limited, OG & C Laboratory, Thane Soil Engineering and Material Testing Wing, Pune Standard (Madras) Laboratories, Chennai Switchgear Testing Laboratories (STL), Larsen & Toubro Limited, Powai, Mumbai Testings Concern, Howrah VXL eTech - EMClSafety Lab, Bangalore
C,M,B
F
C, M, NDT L
E
C,B
C,M
F
C,B
M
C,M
M
C,M
M C C
C,M
C
C,M C,M
C
C,M C,M
E
C,M
L
36
1. 2. 3. 4.
M M
M
M M M M
M
FF
M M
6.
7. 8. 9. 10. 11.
Department of Laboratory Services, B.M. Birla Heart Research Centre, Kolkata Department of Pathology, Calcutta Medical Research Institute, Kolkatta Dr. Vaidya's Laboratory, Thane Dr. Ajay Shah Pathology Laboratory, Mumbai Laboratory Services of Indraprastha Apollo Hospital, New Delhi Manipal Hospital Diagnostic Services, Bangalore MolecularDiagnosticLaboratory, Reliance Life Sciences, Maumbai Madras Diagnostic Centre, Chennai Sipra Labs Limited (Clinical Laboratory), Hyderabad Testing & Cross-Match Laboratories, Prathama Blood Centre. Ahmedabad
Biochemistry, Pathology, Cytopathology, Haematology, Histopathology, Microbiology and Serology Biochemistry, Pathology, Haematology, Serology Biochemistry, Pathology, Haematology Biochemistry, Pathology, Haematology, Cytopathology, Histopathology, Microbiology and Serology Biochemistry, Pathology, Haematology, Cytopathology, Histopathology, Microbiology and Serology Cytogenetics, Immunology Biochemistry, Pathology, Haematology, Microbiology and Serology Biochemistry, Pathology, Haematology, Immunology
Immunology
Abbteoiationsused:C:Chemical,M=Mechanical,E:Electrical,T:Thermal,B:Biological,FF:FluidFlow,
P:Photometry,L:Electronics,F:ForensicTesting,NDT:NonDestructiveTesting,R:Radiological,ET:Electrotechnical, O = Optical, T&O - Thermal & Optical
Scope
" ww w. n
of Accreditation and other detoils of all Accredited abl-i n di a. org" u nder' Labo rato ry Se qrch,.
Lo,[p1r61tories are
37
Document Name
Doc. No.
lssue
No.
lssue
Date Dec. 2004
Last Amend.
No.
'|
NABL
1OO
2.
a
NABL 102
NABL
'|
01
994
o2
01
21.10.03
05 o7 05
Free of cos Free of cos Free of cosl Free ol cost Free of cos Free of cost
03
02 o2
0'1
28.02.o3 02.04.03
1
4.
tr
Specific Criteria for Electrical Testinq Laboratories Specific Criteria for Electronics Testing Laboratories Specific Criteria for Fluid Flow Testing Laboratories Guidelines and Specific Criteria for Accreditation
01
995
994
o2 02 o2
0.t
7.
02
Nov. 1999
NABL 108
01
994
o2
05.07.05
Free of cost
01
April 1998
1
02 02 o2 02
'10
01
994
11
o2
01
11 05.05
12
Specific Guidelines for Accreditation of Forensic Science Laboratories & Checklist for Assessors
NABL 113
18 06.98
13.
rl
Specific Guidelines for Accreditation of DNA Fingerprinting Laboratories & Checklist for Assessor
NABL 113A
01
29.'t2.99
o2
21.10 03
Reinducted
Free of cost
on reqquest
Free of cost
14
NABL
1.14
02 03
05.07.05 08.10.02
00
01
NABL-12.I
05.07.05
Free of Cost
Electro-Technical Discipline
;i
16.
NABL 122
03
08. t 0.02
01
05.07.05
ree of Cost
lir::.::::
38
S. No.
Document Name
Doc. No.
lssue
No.
lssue
Date
Price
(Rs.)
17
NABL,I23
03
08 10.02
0'r
05.07.05
Free of Cos
18
NABL 124
03
08.10.02
02
05.07.05
Free of Cos
19
NABL
,I
25
03
08.10.02
01
05.07.05
Free of Cosl
NABL 130
02
13 08.02
01
05.07 05
Free of Cos
)4
NABL 131
o4
01 .o3.o2
02
05.07.05
Free of Cos'
Accreditation
22.
NABL 133
02
13.07.00
02
13.08.02
Free of cosl
NABL 14,I
02
o2.o4 00
03
18.08.00
Free of Cos
of Uncertainty in Measurement
24 Policy on Calibration and Traceabilitv
NABL 't42
03
't8.'to.o4
o2
05.07.05
Free of Cosl
of Measurements
25.
26 27 28
Application Form for Testing Laboratories Application Form for Calibration Laboratories
Guide for preparing a Quality Manual Guide for Internal Audit and Management Review
09 09 03 02
02
05.07.05 05.07.05
o2 00
02
05.07.05
Free of Cos
for
Guidelines for Proficiency testing programme for Testing & Calibration Laboratories
30
04.04.01
01
05.07.05
Free of Cosl
NABL 163
o4
13.08.02
o4
18.10.04
Free of cosi
'39
S. No.
Document Name
Doc. No.
lssue
No.
lssue
Date 28.04.05
Price (Rs.)
Amend.
31
NABL 164
01
Free of cosl
32.
NABL 174
o2
14.10.O4
01
05.07.05
Free of Cos
JJ
Master list of NABL Documents Pre-Assessment Guidelines and Forms NABL Assessor Guide
NABL
2OO
08
01
0s.07.05
02.12.O2
00
Free of cos
05 o7 05 05 o1 05
34.
35
JO
0t
03 05
03 03
01.05.02 03.o4.o2
05.07.05
37
NABL 215
UJ
0s.07.05
00
Free of cost
38
NABL 216
01
28 10.O2
10
05,07 05
f:ree of cos
Adverse Decisions
39
Bio-data of Assessors
:
NABL 22-I
01
02.08 04
00
05 07.05
['ree of cos
Note
1. 2. 3.
The shaded boxes of a row indicate the new issues or neu/ amendments of the document and the shaded row indicate the new documents published or withdrawn.
All NABL documents can be downloaded free of cost f rm NABL website : www.nabl-india.org The Master list is updated on a reqular basis and is also availaille on NABL wbsite.
:
ECitorial Board
Srikanth
- Member
tiABL NEWS is quarterly published by National Accreditation Board for Testing and Calibration Labc'-ai,,.-'iies (NABL)
B-4 Apartment, Qutab Hotel, New Mehrauli Road, New Delhi - 110016. India Tel.: 011- 26529778- 20,26526864, Fax: 017- 26529776 E-rrail, info@nabl-india.org Website : www.nabl-india.org
Registered Office: Department of Science & Technology, Technology Bhavan, New Mehrauli Road. New Delhi-110016
40