Help Print this page 

Document 32009D0108

Title and reference
2009/108/EC: Commission Decision of 3 February 2009 amending Decision 2002/364/EC on common technical specifications for in vitro -diagnostic medical devices (notified under document number C(2009) 565) (Text with EEA relevance)
  • No longer in force
OJ L 39, 10.2.2009, p. 34–49 (BG, ES, CS, DA, DE, ET, EL, EN, FR, IT, LV, LT, HU, MT, NL, PL, PT, RO, SK, SL, FI, SV)

ELI: http://data.europa.eu/eli/dec/2009/108(1)/oj
Multilingual display
Dates
  • Date of document: 03/02/2009
  • Date of effect: 04/02/2009; Takes effect Date notif.
  • Date of effect: 01/12/2009; Partial application See Art 2
  • Date of effect: 01/12/2010; Partial application See Art 2
  • Date of notification: 04/02/2009
  • Date of end of validity: 29/11/2009; Repealed by 32009D0886
Miscellaneous information
  • Author: European Commission
  • Form: Decision
  • Addressee: The Member States
  • Additional information: EEA relevance
Relationship between documents
Text

10.2.2009   

EN

Official Journal of the European Union

L 39/34


COMMISSION DECISION

of 3 February 2009

amending Decision 2002/364/EC on common technical specifications for in vitro-diagnostic medical devices

(notified under document number C(2009) 565)

(Text with EEA relevance)

(2009/108/EC)

THE COMMISSION OF THE EUROPEAN COMMUNITIES,

Having regard to the Treaty establishing the European Community,

Having regard to Directive 98/79/EC of the European Parliament and of the Council of 27 October 1998 on in vitro-diagnostic medical devices (1), and in particular the second subparagraph of Article 5(3) thereof,

Whereas:

(1)

The common technical specifications for in vitro-diagnostic medical devices are laid down in Commission Decision 2002/364/EC (2).

(2)

In the interest of public health and in order to reflect technical progress including the evolution in the performance and analytical sensitivity of devices, it is appropriate to revise the common technical specifications laid down in Decision 2002/364/EC.

(3)

The definition of rapid test should be refined in order for it to be more precise. For the sake of clarity further definitions should be included.

(4)

To bring the common technical specifications in line with current scientific and technical practices it is necessary to update a number of scientific and technical references.

(5)

The requirements for HIV screening assays should be clarified. In order to ensure that the performance criteria appropriate to today’s technology is reflected in the common technical specifications it is necessary to add requirements for HIV antibody/antigen combined tests and further specification of the sample requirements for certain assays.

(6)

The Annex to Decision 2002/364/EC should therefore be amended accordingly and, for the purpose of clarity, be replaced.

(7)

Manufacturers whose devices are already on the market should be given a transition period in order to adapt to the new common technical specifications. On the other hand, in the interest of public health, manufacturers who so wish should be able to apply the new common technical specifications before the expiry of the transition period.

(8)

The measures provided for in this Decision are in accordance with the opinion of the committee set up by Article 6(2) of Council Directive 90/385/EEC (3),

HAS ADOPTED THIS DECISION:

Article 1

The Annex to Decision 2002/364/EC is replaced by the text in the Annex to this Decision.

Article 2

This Decision shall apply from 1 December 2010 for those devices first placed on the market prior to 1 December 2009.

It shall apply from 1 December 2009 for all other devices.

However, Member States shall allow manufacturers to apply the requirements set out in the Annex before the dates set out in the first and second paragraph.

Article 3

This Decision is addressed to the Member States.

Done at Brussels, 3 February 2009.

For the Commission

Günter VERHEUGEN

Vice-President


(1)  OJ L 331, 7.12.1998, p. 1.

(2)  OJ L 131, 16.5.2002, p. 17.

(3)  OJ L 189, 20.7.1990, p. 17.


ANNEX

‘ANNEX

COMMON TECHNICAL SPECIFICATIONS (CTS) FOR IN VITRO-DIAGNOSTIC MEDICAL DEVICES

1.   SCOPE

The common technical specifications set out in this Annex shall apply for the purposes of Annex II List A to Directive 98/79/EC.

2.   DEFINITIONS AND TERMS

(Diagnostic) sensitivity

The probability that the device gives a positive result in the presence of the target marker.

True positive

A specimen known to be positive for the target marker and correctly classified by the device.

False negative

A specimen known to be positive for the target marker and misclassified by the device.

(Diagnostic) specificity

The probability that the device gives a negative result in the absence of the target marker.

False positive

A specimen known to be negative for the target marker and misclassified by the device.

True negative

A specimen known to be negative for the target marker and correctly classified by the device.

Analytical sensitivity

Analytical sensitivity may be expressed as the limit of detection, i.e. the smallest amount of the target marker that can be precisely detected.

Analytical specificity

Analytical specificity means the ability of the method to determine solely the target marker.

Nucleic acid amplification techniques (NAT)

The term “NAT” is used for tests for the detection and/or quantification of nucleic acids by either amplification of a target sequence, by amplification of a signal or by hybridisation.

Rapid test

“Rapid test” means qualitative or semi-quantitative in vitro-diagnostic medical devices, used singly or in a small series, which involve non-automated procedures and have been designed to give a fast result.

Robustness

The robustness of an analytical procedure means the capacity of an analytical procedure to remain unaffected by small but deliberate variations in method parameters and provides an indication of its reliability during normal usage.

Whole system failure rate

The whole system failure rate means the frequency of failures when the entire process is performed as prescribed by the manufacturer.

Confirmation assay

Confirmation assay means an assay used for the confirmation of a reactive result from a screening assay.

Virus typing assay

Virus typing assay means an assay used for typing with already known positive samples, not used for primary diagnosis of infection or for screening.

Seroconversion HIV samples

Seroconversion HIV samples mean:

p24 antigen and/or HIV RNA positive, and

recognised by all of the antibody screening tests, and

positive or indeterminate confirmatory assays,

Early seroconversion HIV samples

Early seroconversion HIV samples mean:

p24 antigen and/or HIV RNA positive, and

not recognised by all of the antibody screening tests, and

indeterminate or negative confirmatory assays.

3.   COMMON TECHNICAL SPECIFICATIONS (CTS) FOR PRODUCTS REFERRED TO IN ANNEX II, LIST A OF DIRECTIVE 98/79/EC

3.1.   CTS for performance evaluation of reagents and reagent products for the detection, confirmation and quantification in human specimens of markers of HIV infection (HIV 1 and 2), HTLV I and II, and hepatitis B, C, D

General Principles

3.1.1.   Devices which detect virus infections placed on the market for use as either screening or diagnostic tests, shall meet the requirements for sensitivity and specificity set out in Table 1. See also principle 3.1.11 for screening assays.

3.1.2.   Devices intended by the manufacturer for testing body fluids other than serum or plasma, e.g. urine, saliva, etc. shall meet the same CTS requirements for sensitivity and specificity as serum or plasma tests. The performance evaluation shall test samples from the same individuals in both the tests to be approved and in a respective serum or plasma assay.

3.1.3.   Devices intended by the manufacturer for self-test, i.e. home use shall meet the same CTS requirements for sensitivity and specificity as respective devices for professional use. Relevant parts of the performance evaluation shall be carried out (or repeated) by appropriate lay users to validate the operation of the device and the instructions for use.

3.1.4.   All performance evaluations shall be carried out in direct comparison with an established state-of-the-art device. The device used for comparison shall be one bearing CE marking, if on the market at the time of the performance evaluation.

3.1.5.   If discrepant test results are identified as part of an evaluation, these results shall be resolved as far as possible, for example:

by evaluation of the discrepant sample in further test systems,

by use of an alternative method or marker,

by a review of the clinical status and diagnosis of the patient, and

by the testing of follow-up-samples.

3.1.6.   Performance evaluations shall be performed on a population equivalent to the European population.

3.1.7.   Positive specimens used in the performance evaluation shall be selected to reflect different stages of the respective disease(s), different antibody patterns, different genotypes, different subtypes, mutants, etc.

3.1.8.   Sensitivity with true positives and seroconversion samples shall be evaluated as follows:

3.1.8.1.

Diagnostic test sensitivity during seroconversion has to represent the state of the art. Whether further testing of the same or additional seroconversion panels is conducted by the notified body or by the manufacturer the results shall confirm the initial performance evaluation data (see Table 1). Seroconversion panels should start with a negative bleed(s) and should have narrow bleeding intervals.

3.1.8.2.

For blood screening devices (with the exception of HBsAg and anti-HBc tests), all true positive samples shall be identified as positive by the device to be CE marked (Table 1). For HBsAg and anti-HBc tests the new device shall have an overall performance at least equivalent to that of the established device (see 3.1.4).

3.1.8.3.

Regarding HIV tests:

all seroconversion HIV samples shall be identified as positive, and

at least 40 early seroconversion HIV samples shall be tested. Results should conform to the state of the art.

3.1.9.   Performance evaluation of screening assays shall include 25 positive (if available in the case of rare infections) “same day” fresh serum and/or plasma samples (≤ 1 day after sampling).

3.1.10.   Negative specimens used in a performance evaluation shall be defined so as to reflect the target population for which the test is intended, for example blood donors, hospitalised patients, pregnant women, etc.

3.1.11.   For performance evaluations for screening assays (Table 1) blood donor populations shall be investigated from at least two blood donation centres and consist of consecutive blood donations, which have not been selected to exclude first-time donors.

3.1.12.   Devices shall have a specificity of at least 99,5 % on blood donations, unless otherwise indicated in the accompanying tables. Specificity shall be calculated using the frequency of repeatedly reactive (i.e. false positive) results in blood donors negative for the target marker.

3.1.13.   Devices shall be evaluated to establish the effect of potential interfering substances, as part of the performance evaluation. The potential interfering substances to be evaluated will depend to some extent on the composition of the reagent and configuration of the assay. Potential interfering substances shall be identified as part of the risk analysis required by the essential requirements for each new device but may include, for example:

specimens representing “related” infections,

specimens from multipara, i.e. women who have had more than one pregnancy, or rheumatoid factor positive patients,

for recombinant antigens, human antibodies to components of the expression system, for example anti-E. coli, or anti-yeast,

3.1.14.   For devices intended by the manufacturer to be used with serum and plasma the performance evaluation must demonstrate serum to plasma equivalency. This shall be demonstrated for at least 50 donations (25 positive and 25 negative).

3.1.15.   For devices intended for use with plasma the performance evaluation shall verify the performance of the device using all anticoagulants which the manufacturer indicates for use with the device. This shall be demonstrated for at least 50 donations (25 positive and 25 negative).

3.1.16.   As part of the required risk analysis the whole system failure rate leading to false-negative results shall be determined in repeat assays on low-positive specimens.

3.1.17.   If a new in vitro-diagnostic medical device belonging to Annex II List A is not specifically covered by the common technical specification, the common technical specification for a related device should be taken into account. Related devices may be identified on different grounds, e.g. by the same or similar intended use or by similar risks.

3.2.   Additional Requirements for HIV antibody/antigen combined tests

3.2.1.   HIV antibody/antigen combined tests intended for anti-HIV and p24 antigen detection which include claims for single p24 antigen detection shall follow Table 1 and Table 5, including criteria for analytical sensitivity for p24 antigen.

3.2.2.   HIV antibody/antigen combined tests intended for anti-HIV and p24 detection which do not include claims for single p24 detection shall follow Table 1 and Table 5, excluding criteria for analytical sensitivity for p24.

3.3.   Additional Requirements for Nucleic Acid Amplification Techniques (NAT)

The performance evaluation criteria for NAT assays can be found in Table 2.

3.3.1.   For target sequence amplification assays, a functionality control for each test sample (internal control) shall reflect the state of the art. This control shall as far as possible be used throughout the whole process, i.e. extraction, amplification/hybridisation, detection.

3.3.2.   The analytical sensitivity or detection limit for NAT assays shall be expressed by the 95 % positive cut-off value. This is the analyte concentration where 95 % of test runs give positive results following serial dilutions of an international reference material for example a WHO standard or calibrated reference material.

3.3.3.   Genotype detection shall be demonstrated by appropriate primer or probe design validation and shall also be validated by testing characterised genotyped samples.

3.3.4.   Results of quantitative NAT assays shall be traceable to international standards or calibrated reference materials, if available, and be expressed in international units utilised in the specific field of application.

3.3.5.   NAT assays may be used to detect virus in antibody negative samples, i.e. pre-seroconversion samples. Viruses within immune-complexes may behave differently in comparison to free viruses, for example during a centrifugation step. It is therefore important that during robustness studies, antibody-negative (pre-seroconversion) samples are included.

3.3.6.   For investigation of potential carry-over, at least five runs with alternating high-positive and negative specimens shall be performed during robustness studies. The high positive samples shall comprise of samples with naturally occurring high virus titres.

3.3.7.   The whole system failure rate leading to false-negative results shall be determined by testing low-positive specimens. Low positive specimens shall contain a virus concentration equivalent to three times the 95 % positive cut-off virus concentration.

3.4.   CTS for the manufacturer’s release testing of reagents and reagent products for the detection, confirmation and quantification in human specimens of markers of HIV infection (HIV 1 and 2), HTLV I and II, and hepatitis B, C, D (Immunological assays only)

3.4.1.   The manufacturers release testing criteria shall ensure that every batch consistently identifies the relevant antigens, epitopes, and antibodies.

3.4.2.   The manufacturer’s batch release testing for screening assays shall include at least 100 specimens negative for the relevant analyte.

3.5.   CTS for performance evaluation of reagents and reagent products for determining the following blood group antigens: ABO blood group system ABO1 (A), ABO2 (B), ABO3 (A,B); Rh blood group system RH1 (D), RH2 (C), RH3 (E), RH4 (c), RH5 (e); Kell blood group system KEL1 (K)

Criteria for performance evaluation of reagents and reagent products for determining the blood groups antigens: ABO blood group system ABO1 (A), ABO2 (B), ABO3 (A,B); Rh blood group system RH1 (D), RH2 (C), RH3 (E), RH4 (c), RH5 (e); Kell blood group system KEL1 (K) can be found in Table 9.

3.5.1.   All performance evaluations shall be carried out in direct comparison with an established state-of-the-art device. The device used for comparison shall be one bearing CE marking, if on the market at the time of the performance evaluation.

3.5.2.   If discrepant test results are identified as part of an evaluation, these results shall be resolved as far as possible, for example:

by evaluation of the discrepant sample in further test systems,

by use of an alternative method,

3.5.3.   Performance evaluations shall be performed on a population equivalent to the European population.

3.5.4.   Positive specimens used in the performance evaluation shall be selected to reflect variant and weak antigen expression.

3.5.5.   Devices shall be evaluated to establish the effect of potential interfering substances, as part of the performance evaluation. The potential interfering substances to be evaluated will depend to some extent on the composition of the reagent and configuration of the assay. Potential interfering substances shall be identified as part of the risk analysis required by the essential requirements for each new device.

3.5.6.   For devices intended for use with plasma the performance evaluation shall verify the performance of the device using all anticoagulants which the manufacturer indicates for use with the device. This shall be demonstrated for at least 50 donations.

3.6.   CTS for the manufacturers release testing of reagents and reagent products for determining the blood group antigens: ABO blood group system ABO1 (A), ABO2 (B), ABO3 (A,B); Rh blood group system RH1 (D), RH2 (C), RH3 (E), RH4 (c), RH5 (e); Kell blood group system KEL1 (K)

3.6.1.   The manufacturer’s release testing criteria shall ensure that every batch consistently identifies the relevant antigens, epitopes, and antibodies.

3.6.2.   Requirements for manufacturers batch release testing are outlined in Table 10.

Table 1

“Screening” assays: anti-HIV 1 and 2, anti-HTLV I and II, anti-HCV, HBsAg, anti-HBc

 

 

Anti-HIV-1/2

Anti-HTLV-I/II

Anti-HCV

HBsAg

Anti-HBc

Diagnostic sensitivity

Positive specimens

400 HIV-1

100 HIV-2

including 40 non-B-subtypes, all available HIV/1 subtypes should be represented by at least 3 samples per subtype

300 HTLV-I

100 HTLV-II

400 (positive samples)

Including samples from different stages of infection and reflecting different antibody patterns.

Genotype 1-4: > 20 samples per genotype (including non-a sub-types of genotype 4);

5: > 5 samples;

6: if available

400

Including subtype-consideration

400

Including evaluation of other HBV-markers

Seroconversion panels

20 panels

10 further panels (at Notified Body or manufacturer)

To be defined when available

20 panels

10 further panels (at Notified Body or manufacturer)

20 panels

10 further panels (at Notified Body or manufacturer)

To be defined when available

Analytical sensitivity

Standards

 

 

 

0,130 IU/ml (Second International Standard for HBsAg, subtype adw2, genotype A, NIBSC code: 00/588)

 

Specificity

Unselected donors (including first-time donors)

5 000

5 000

5 000

5 000

5 000

Hospitalised patients

200

200

200

200

200

Potentially cross-reacting blood-specimens (RF+, related viruses, pregnant women, etc.)

100

100

100

100

100


Table 2

NAT assays for HIV1, HCV, HBV, HTLV I/II (qualitative and quantitative; not molecular typing)

HIV1

HCV

HBV

HTLV I/II

Acceptance criteria

NAT

qualitative

quantitative

qualitative

quantitative

qualitative

quantitative

qualitative

quantitative

As for HIV quantitative

As for HIV quantitative

As for HIV quantitative

Sensitivity Detection limit Detection of analytical sensitivity (IU/ml; defined on WHO standards or calibrated reference materials)

According to EP validation guideline (1): several dilution series into borderline concentration; statistical analysis (e.g. Probit analysis) on the basis of at least 24 replicates; calculation of 95 % cut-off value

Detection limit: as for qualitative tests; Quantification limit: dilutions (half-log10 or less) of calibrated reference preparations, definition of lower, upper quantification limit, precision, accuracy, “linear” measuring range, “dynamic range”. Reproducibility at different concentration levels to be shown

According to EP validation guideline (1): several dilution series into borderline concentration; statistical analysis (e.g. Probit analysis) on the basis of at least 24 replicates; calculation of 95 % cut-off value

 

According to EP validation guideline (1): several dilution series into borderline concentration; statistical analysis (e.g. Probit analysis) on the basis of at least 24 replicates; calculation of 95 % cut-off value

 

According to EP validation guideline (1): several dilution series into borderline concentration; statistical analysis (e.g. Probit analysis) on the basis of at least 24 replicates; calculation of 95 % cut-off value

 

 

Genotype/subtype detection/quantification efficiency

At least 10 samples per subtype (as far as available)

Dilution series of all relevant genotypes/subtypes, preferably of reference materials, as far as available

At least 10 samples per genotype (as far as available)

 

As far as calibrated genotype reference materials are available

 

As far as calibrated genotype reference materials are available

 

 

Cell culture supernatants (could substitute for rare HIV-1 subtypes)

Transcripts or plasmids quantified by appropriate methods may be used.

 

 

 

 

 

 

 

According to EP validation guideline (1) as far as calibrated subtype reference materials are available; in vitro transcripts could be an option

 

According to EP validation guideline (1) as far as calibrated subtype reference materials are available; in vitro transcripts could be an option

 

According to EP validation guideline (1) as far as calibrated subtype reference materials are available; in vitro transcripts could be an option

 

According to EP validation guideline (1) as far as calibrated subtype reference materials are available; in vitro transcripts could be an option

 

 

Diagnostic specificity negative samples

500 blood donors

100 blood donors

500 blood donors

 

500 blood donors

 

500 individual blood donations

 

 

Potential cross-reactive markers

By suitable assay design evidence (e.g. sequence comparison) and/or testing of at least 10 human retrovirus (e.g. HTLV)-positive samples

As for qualitative tests

By assays design and/or testing of at least 10 human flavivirus (e.g. HGV, YFV) positive samples

 

By assays design and/or testing of at least 10 other DNA-virus positive samples

 

By assay design and/or testing of at least 10 human retrovirus (e.g. HIV-) positive samples

 

 

Robustness

 

As for qualitative tests

 

 

 

 

 

 

 

Cross-contamination

At least 5 runs using alternating high positive (known to occur naturally) and negative samples

 

At least 5 runs using alternating high positive (known to occur naturally) and negative samples

 

At least 5 runs using alternating high positive (known to occur naturally) and negative samples

 

At least 5 runs using alternating high positive (known to occur naturally) and negative samples

 

 

Inhibition

Internal control preferably to go through the whole NAT procedure

 

Internal control preferably to go through the whole NAT procedure

 

Internal control preferably to go through the whole NAT procedure

 

Internal control preferably to go through the whole NAT procedure

 

 

Whole system failure rate leading to false-neg results

At least 100 samples virus-spiked with 3 x the 95 % pos cut-off concentration

 

At least 100 samples virus-spiked with 3 x the 95 % pos cut-off concentration

 

At least 100 samples virus-spiked with 3 x the 95 % pos cut-off concentration

 

At least 100 samples virus-spiked with 3 x the 95 % pos cut-off concentration

 

99/100 assays positive

Notes: Acceptance criteria for “whole system failure rate leading to false-neg results” is 99/100 assays positive.

For quantitative NATs a study shall be performed on at least 100 positive specimens reflecting the routine conditions of users (e.g. no pre-selection of specimens). Comparative results with another NAT test system shall be generated in parallel.

For qualitative NATs a study on diagnostic sensitivity shall be performed using at least 10 seroconversion panels. Comparative results with another NAT test system shall be generated in parallel.


Table 3

Rapid tests: anti-HIV 1 and 2, anti-HCV, HBsAg, anti-HBc, anti-HTLV I and II

 

 

Anti-HIV 1/2

Anti-HCV

HBsAg

Anti-HBc

anti-HTLV I/II

Acceptance criteria

Diagnostic sensitivity

Positive specimens

Same criteria as for screening assays

Same criteria as for screening assays

Same criteria as for screening assays

Same criteria as for screening assays

Same criteria as for screening assays

Same criteria as for screening assays

Seroconversion panels

Same criteria as for screening assays

Same criteria as for screening assays

Same criteria as for screening assays

Same criteria as for screening assays

Same criteria as for screening assays

Same criteria as for screening assays

Diagnostic specificity

Negative specimens

1 000 blood donations

1 000 blood donations

1 000 blood donations

1 000 blood donations

1 000 blood donations

≥ 99 % (anti-HBc: ≥ 96 %)

200 clinical specimens

200 clinical specimens

200 clinical specimens

200 clinical specimens

200 clinical specimens

200 samples from pregnant women

200 samples from pregnant women

200 samples from pregnant women

 

200 samples from pregnant women

100 potentially interfering samples

100 potentially interfering samples

100 potentially interfering samples

100 potentially interfering samples

100 potentially interfering samples


Table 4

Confirmatory/supplementary assays for anti-HIV 1 and 2, anti-HTLV I and II, anti-HCV, HBsAg

 

 

Anti-HIV Confirmatory Assay

Anti-HTLV Confirmatory Assay

HCV Supplementary Assay

HBsAg Confirmatory Assay

Acceptance criteria

Diagnostic sensitivity

Positive specimens

200 HIV-1 and 100 HIV-2

200 HTLV-I and 100 HTLV-II

300 HCV (positive samples)

300 HBsAg

Correct identification as positive (or indeterminate), not negative

Including samples from different stages of infection and reflecting different antibody patterns

 

Including samples from different stages of infection and reflecting different antibody patterns.

Genotypes 1 – 4: > 20 samples (including non-a sub-types of genotype 4);

5: > 5 samples;

6: if available

Including samples from different stages of infection

20 “high pos” samples (> 26 IU/ml); 20 samples in the cut-off range

 

Seroconversion panels

15 seroconversion panels/low titre panels

 

15 seroconversion panels/low titre panels

15 seroconversion panels/low titre panels

 

Analytical sensitivity

Standards

 

 

 

Second International Standard for HBsAg, subtype adw2, genotype A, NIBSC code: 00/588

 

Diagnostic specificity

Negative specimens

200 blood donations

200 blood donation

200 blood donations

10 false positives as available from the performance evaluation of the screening assay. (2)

No false-positive results/ (2) no neutralisation

200 clinical samples including pregnant women

200 clinical samples including pregnant women

200 clinical samples including pregnant women

 

 

50 potentially interfering samples, including samples with indeterminate results in other confirmatory assays

50 potentially interfering samples including samples with indeterminate results in other confirmatory assays

50 potentially interfering samples including samples with indeterminate results in other supplementary assays

50 potentially interfering samples

 


Table 5

HIV 1 Antigen

 

HIV-1 Antigen Assay

Acceptance criteria

Diagnostic sensitivity

Positive specimens

50 HIV-1 Ag-positive

50 cell culture supernatants including different HIV-1 subtypes and HIV-2

Correct identification (after neutralisation)

Seroconversion panels

20 seroconversion panels/low titre panels

 

Analytical sensitivity

Standards

HIV-1 p24 Antigen, 1st International Reference Reagent, NIBSC code: 90/636

≤ 2 IU/ml

Diagnostic specificity

 

200 blood donations

200 clinical samples

50 potentially interfering samples

≥ 99,5 % after neutralisation


Table 6

Serotyping and Genotyping Assay: HCV

 

HCV Serotyping and Genotyping Assay

Acceptance criteria

Diagnostic sensitivity

Positive specimens

200 (positive samples)

Including samples from different stages of infection and reflecting different antibody patterns.

Genotypes 1 – 4: ≥ 20 samples (including non-a sub-types of genotype 4);

5: ≥ 5 samples;

6: if available

≥ 95 % agreement between serotyping and genotyping

≥ 95 % agreement between genotyping and sequencing

Diagnostic specificity

Negative specimens

100

 


Table 7

HBV Markers: anti-HBs, anti-HBc IgM, anti-HBe, HBeAg

 

Anti-HBs

Anti-HBc IgM

Anti-HBe

HBeAg

Acceptance criteria

Diagnostic sensitivity

Positive specimens

100 vaccinees

200

200

200

≥ 98 %

100 naturally infected persons

Including samples from different stages of infection (acute/chronic, etc.)

The acceptance criteria should only be applied on samples from acute infection stage.

Including samples from different stages of infection (acute/chronic, etc.)

Including samples from different stages of infection (acute/chronic, etc.)

Seroconversion panels

10 follow-ups or anti-HBs seroconversions

When available

 

 

 

Analytical sensitivity

Standards

WHO 1st International Reference Preparation 1977; NIBSC, United Kingdom

 

 

HBe – Referenzantigen 82; PEI Germany

Anti-HBs: < 10 mIU/ml

Diagnostic specificity

Negative specimens

500

200 blood donations

200 blood donation

200 blood donations

≥ 98 %

Including clinical samples 50 potentially interfering samples

200 clinical samples 50 potentially interfering samples

200 clinical samples 50 potentially interfering samples

200 clinical samples 50 potentially interfering samples


Table 8

HDV markers: anti-HDV, anti-HDV IgM, Delta Antigen

 

Anti-HDV

Anti-HDV IgM

Delta Antigen

Acceptance criteria

Diagnostic sensitivity

Positive specimens

100

50

10

≥ 98 %

Specifying HBV-markers

Specifying HBV-markers

Specifying HBV-markers

Diagnostic specificity

Negative specimens

200

200

200

≥ 98 %

Including clinical samples

Including clinical samples

Including clinical samples

50 potentially interfering samples

50 potentially interfering samples

50 potentially interfering samples


Table 9

Blood group antigens in the ABO, Rh and Kell blood group systems

 

1

2

3

Specificity

Number of tests per recommended method

Total number of samples to be tested for a launch product

Total number of samples to be tested for a new formulation, or use of well-characterised reagents

Anti-ABO1 (anti-A), anti-ABO2 (anti-B), anti-ABO3 (anti-A,B)

500

3 000

1 000

Anti-RH1 (anti-D)

500

3 000

1 000

Anti-RH2 (anti-C), anti-RH4 (anti-c), anti-RH3 (anti-E)

100

1 000

200

Anti-RH5 (anti-e)

100

500

200

Anti-KEL1 (anti-K)

100

500

200

Acceptance criteria:

All of the above reagents shall show comparable test results with established reagents with acceptable performance with regard to claimed reactivity of the device. For established reagents, where the application or use has been changed or extended, further testing should be carried out in accordance with the requirements outlined in column 1 (above).

Performance evaluation of anti-D-reagents shall include tests against a range of weak RH1 (D) and partial RH1 (D) samples, depending on the intended use of the product.

Qualifications:

Clinical samples

:

10 % of the test population

Neonatal specimens

:

> 2 % of the test population

ABO samples

:

> 40 % A, B positives

“weak D”

:

> 2 % of RH1 (D) positives

Table 10

Batch release criteria for reagents and reagent products to determine blood group antigens in the ABO, Rh and Kell blood group systems

Specificity Testing Requirements on each reagent

1.   Test reagents

Blood Group Reagents

Minimum number of control cells to be tested

 

Positive reactions

 

Negative reactions

 

A1

A2B

Ax

 

 

B

0

 

Anti-ABO1 (anti-A)

2

2

2 (3)

 

2

2

 

 

B

A1B

 

 

A1

0

 

Anti-ABO2 (anti-B)

2

2

 

 

2

2

 

 

A1

A2

Ax

B

0

 

 

Anti-ABO3 (anti-A,B)

2

2

2

2

4

 

 

 

 

 

 

 

 

 

 

 

R1r

R2r

WeakD

 

r’r

r’’r

rr

Anti-RH1 (anti-D)

2

2

2 (3)

 

1

1

1

 

R1R2

R1r

r’r

 

R2R2

r’’r

rr

Anti-RH2 (anti-C)

2

1

1

 

1

1

1

 

R1R2

R1r

r’r

 

R1R1

 

 

Anti-RH4 (anti-c)

1

2

1

 

3

 

 

 

R1R2

R2r

r’’r

 

R1R1

r’r

rr

Anti-RH 3 (anti-E)

2

1

1

 

1

1

1

 

R1R2

R2r

r’’r

 

R2R2

 

 

Anti-RH5 (anti-e)

2

1

1

 

3

 

 

 

Kk

 

 

 

kk

 

 

Anti-KEL1 (anti-K)

4

 

 

 

3

 

 

Note: Polyclonal reagents must be tested against a wider panel of cells to confirm specificity and exclude presence of unwanted contaminating antibodies.

Acceptance Criteria:

Each batch of reagent must exhibit unequivocal positive or negative results by all recommended techniques in accordance with the results obtained from the performance evaluation data.

2.   Control Materials (red Cells)

The phenotype of red cells used in the control of blood typing reagents listed above should be confirmed using established device.’


(1)  European Pharmacopoeia guideline.

Notes: Acceptance criteria for “whole system failure rate leading to false-neg results” is 99/100 assays positive.

For quantitative NATs a study shall be performed on at least 100 positive specimens reflecting the routine conditions of users (e.g. no pre-selection of specimens). Comparative results with another NAT test system shall be generated in parallel.

For qualitative NATs a study on diagnostic sensitivity shall be performed using at least 10 seroconversion panels. Comparative results with another NAT test system shall be generated in parallel.

(2)  Acceptance criteria no neutralisation for HBsAg confirmatory assay.

(3)  Only by recommended techniques where reactivity against these antigens is claimed.

Note: Polyclonal reagents must be tested against a wider panel of cells to confirm specificity and exclude presence of unwanted contaminating antibodies.


Top