2012-01-06
Added
Institutions using the Advanced Measurement Approach for operational risk must establish and submit an AMA Change Policy to competent authorities, classifying extensions and modifications as significant, major, or minor. Extensions and significant changes require explicit prior approval from competent authorities, whereas major and minor changes must be notified and implemented only after receiving an affirmative reply or absence of objection. Competent authorities are required to apply these guidelines and notify the EBA of their compliance by 6 March 2012.
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EBA Guidelines on
Advanced Measurement Approach (AMA) -
Extensions and Changes
(EBA/GL/2012/01)
London, 6 January 2012
Contents
I. Executive Summary........................................................................ 3
II. Background and rationale .............................................................. 5
III. EBA Guidelines on Advanced Measurement Approach (AMA) -
Extensions and Changes .................................................... 7
Title I - Subject matter and scope ....................................................... 9
Title II- Requirements regarding AMA extensions and changes................ 9
Title III- Final Provisions and Implementation ..................................... 12
Annex 1 – Criteria for classification of extensions and changes into,
significant, major and minor changes................................................. 13
IV. Accompanying documents............................................................ 15
Cost- Benefit Analysis / Impact Assessment........................................ 15
Feedback on the public consultation and on the opinion of the BSG ....... 18
V. Form for Confirmation, on the part of Competent Authorities, of
Compliance with these Guidelines ............................................... 29
I. Executive Summary
main issue raised was that it would be beneficial to clarify the categories of major and significant changes. It was also suggested that a definition of more concrete quantitative criteria for distinguishing between major changes and significant changes would be useful. These suggestions were partly taken into account in the finalisation of these Guidelines. However, a common quantitative threshold was not set. The implementation of this aspect will be reviewed by the EBA and taken into account when binding technical standards on the conditions for assessing the materiality of extensions and changes to the AMA will be developed.
6. The EBA conducted a cost and benefit analysis, considering the costs for
institutions and competent authorities. The implementation of the Guidelines is expected to trigger low one-off costs for AMA institutions and competent authorities, especially as the Guidelines only affect a limited number of EU banking groups and institutions using an Advanced Measurement Approach (AMA) for the calculation of the capital requirements for operational risk. Clear communication rules are expected to lead to a smoother process, avoiding case-by-case decisions on the appropriateness of a process and reduce the cost for home/host coordination of competent authorities regarding this matter. Institutions will have more legal certainty about AMA changes being in line with supervisory requirements. An impact on the economy of the EU or a single member state is not expected. The costs of the Guidelines are not unreasonable, as a more consistent treatment of AMA changes will be achieved throughout the EU.
7. Competent authorities should undertake all steps to apply the EBA
Guidelines on the Advanced Measurement Approach (AMA) - Extensions and changes by 6 March 2012, as mentioned in title III thereof.
II. Background and rationale
financial holding company, competent authorities will follow the procedures envisaged by Art. 129 paragraph 2 of Directive 2006/48/EC. The responsibility for organising and coordinating the approval process for extensions and significant changes to the AMA are with the consolidating supervisor.
9. Changes to the AMA and to the quantitative methods used can be of
differing degree of importance, or materiality, depending on the individual AMA. Depending on the materiality of an actual change (i.e. depending on whether this change constitutes an extension or a significant change, or a major or minor change ), different requirements for communication with the competent authorities are provided by these Guidelines.
10. Minor changes are those changes which may occur more often, but
which do not have a severe impact on the reliability of the AMA framework or the capital charge. However, such changes also need to meet the requirements set out in Annex X, Part 3 of Directive 2006/48/EC. Further, a per se insignificant change, in conjunction with other changes, might have a significant impact and, in such cases, needs to be considered accordingly.
11. While extensions and significant changes require prior approval, major
and minor changes need to be notified to the competent authority. Different processes were chosen to reduce the number of approval processes needed and the connected costs and to allow institutions to adopt smaller changes in a timely manner. Institutions need to document the internal procedures and responsibilities for extensions and changes in an AMA change policy.
12. The Annex to these Guidelines elaborates on the criteria for the
classification of extensions and changes in the different categories mentioned above. The criteria that an institution provides for in its AMA Change Policy are expected to be broader than those outlined in the Annex, taking into account the institution’s individual AMA particularities. Given the young and evolutionary nature of operational risk as a risk discipline, this was deemed the preferred approach, given that banks combine the required elements contained within the AMA framework, in a large variety of ways.
13. On 20 July 2011, the European Commission (EC) adopted legislative
proposals, with the view to strengthening the regulation of the banking sector. These proposals contain a requirement for the EBA to develop draft regulatory technical standards to specify the conditions for assessing the materiality of extensions and changes to the AMA. According to this proposal, the EBA shall submit the draft regulatory technical standard to the Commission by 31 December 2013.
14. The implementation of the Guidelines and the experience gained by
assessing model changes according to these Guidelines will be beneficial for developing the future draft regulatory technical standard.
III. EBA Guidelines on Advanced Measurement
Approach (AMA) - Extensions and Changes
(EBA/GL/2012/01)
Status of the Guidelines
In between the text of the Guidelines that follows, further explanations on specific aspects of the guidelines are occasionally provided, which either offer examples or provide the rationale behind a provision. Where this is the case, this explanatory text appears in a framed text box. Contents
Title I - Subject matter and scope ......................................................... 9
Subject matter.................................................................................. 9
Scope and level of application ............................................................. 9
Title II- Requirements regarding AMA extensions and changes ............ 9
AMA Change Policy ............................................................................ 9
Categories of changes to the AMA according to their materiality............ 10
Submission of the AMA Change Policy ................................................ 10
Supervisory procedures for extensions and significant changes ............. 11
Supervisory procedures for major changes ......................................... 11
Supervisory procedures for minor changes ......................................... 12
Title III- Final Provisions and Implementation.................................... 12
Transitional provisions ..................................................................... 12
Date of application .......................................................................... 12
Annex 1 – Criteria for classification of extensions and changes into,
significant, major and minor changes.................................................. 13
A) Extensions to the AMA framework ................................................. 13
B) Significant changes to the AMA ..................................................... 13
C) Major changes to the AMA............................................................ 14
D) Minor changes to the AMA............................................................ 14
Title I - Subject matter and scope
Article 1
Subject matter
These Guidelines harmonise practices and procedures for the internal practices of institutions and for the supervisory treatment of extensions and changes to an Advanced Measurement Approach (‘AMA’) used for determining the regulatory capital charge for operational risk.
Article 2
Scope and level of application
These Guidelines apply to competent authorities and institutions using an AMA for the purpose of calculating the capital requirement for operational risk and, if the AMA is used on a unified basis, to the EU parent credit institution or the EU parent financial holding company. Title II- Requirements regarding AMA extensions and changes
Article 3
AMA Change Policy
An institution should approve at the appropriate hierarchy level, and
should implement, internal policies for AMA extensions and changes (AMA Change Policy), including procedures and responsibilities for the internal approval of AMA extensions and changes, taking into account its organisational characteristics and AMA specificities.
Within an AMA Change Policy, the institution should document its
principles and procedures for classifying and processing planned AMA extensions and changes. This should include appropriate criteria for the classification of possible changes and the internal processes and responsibilities for implementing and documenting AMA extensions and changes.
The classification of planned AMA extensions and changes should be
made into the four categories described below (under article 4). The basic criteria for the classification of planned AMA extensions and changes are elaborated in the Annex to these Guidelines. Nevertheless, institutions should include in their AMA change policy only the criteria which are applicable to their specific AMA, and should develop further criteria than those described in the Annex, taking into account the particularities applying to their AMA.
Further, the AMA Change Policy should provide for an internal or
external independent review of planned extensions or significant changes.
The institution should re-examine and adjust the AMA Change Policy
to reflect changes within its internal governance or AMA framework as appropriate.
The AMA Change Policy and its application should be subject to
regular independent review.
Article 4
Categories of changes to the AMA according to their materiality
The AMA Change Policy should use the following categories of
extensions and changes:
a. Extensions; b. Significant changes;
c. Major changes; and
d. Minor changes.
The classification of any intended change should not be considered
in isolation but it should instead be assessed in connection with other changes that have been made previously, that are intended to take effect at the same time, or changes that are already planned for the future.
The categories and to the extent applicable to each institution the
classification criteria of the different types of changes mentioned above should be integrated in the internal AMA Change Policy. The institution should add further details to the AMA Change Policy consistent with the characteristics of the institution’s internal governance and AMA framework.
In cases where the classification of a change based on the actual
quantitative impact on the regulatory capital and the classification of the same change based on qualitative criteria are different, institutions should classify the relevant change in the category of higher materiality.
Irrespective of the criteria provided for the classification of possible
changes in an institution’s AMA Change Policy, competent authorities retain the right to reclassify the materiality of an actual AMA change and apply the respective supervisory procedures according to these Guidelines.
Article 5
Submission of the AMA Change Policy
The institution or, if the AMA is used on a unified basis, the EU parent
credit institution or the EU parent financial company, should submit its AMA Change Policy and any subsequent modification to the competent authority.
Institutions applying to use an AMA should also submit to
competent authorities an AMA Change Policy as part of the required documentation.
Article 6
Supervisory procedures for extensions and significant changes
including the outline of the change, its rationale, objective and effects on the AMA regulatory capital.
2. The competent authority should evaluate the AMA change and inform
the institution of any regulatory objections to the change. This may entail recommended or mandatory remedial actions, suggestions for the possible improvement of the new/changed parts, or other specific requests (e.g. a parallel running of the old and new AMA framework) and their rationale.
3. The institution should apply the change for regulatory purposes only after
receiving an affirmative reply from the competent authorities.
4. If the competent authority reclassifies the change as an extension or as a
significant change, it should inform the institution, and a separate formal application and approval process should be carried out as required under
Article 6.
Article 8
Supervisory procedures for minor changes
institution.
Annex 1 – Criteria for classification of extensions and changes into,
significant, major and minor changes
This Annex provides a non-exhaustive list of cases that are classified as extensions, and significant, major and minor changes. This list acts as a guide to classify changes according to their materiality. A) Extensions to the AMA framework
changes in the distributional assumptions/parameter estimation procedure), or to important changes within the group structure (e.g. abandonment of significant business units, including subsidiaries);
c. Changes in the logics and drivers of the allocation mechanism;
and d. Fundamental changes in the organisational and operational structure of the operational risk management function, in particular if they impinge on their independence (e.g. measures creating conflicts of interest or limiting the availability of resources). C) Major changes to the AMA Major changes to the AMA include:
a. Changes to the institution’s internal procedures for collecting internal loss data, performing scenario analysis and determining business environment and internal control factors; b. Changes to the measurement system due to modification in the logics or methods, or to changes in the group structure (e.g. changes of the reference date and/or the observation period for building the calculation data set, changes in the criteria/techniques to set the de minimis and/or body-tail modelling thresholds, changes in the granularity of the model, changes in the criteria/techniques for the determination of - previously approved - expected losses, mitigation techniques and recognised correlations.); Explanatory note:
The de minimis modelling threshold represents the level of the losses above which the model is fitted to the data; the body-tail modelling threshold represents the level of the losses which distinguishes the body and tail regions, typically fitted by different methods.
c. Relevant changeover of IT systems for the AMA framework, data
administration or reporting procedures; d. Changes to the institution’s logic and methods used for internally validating and reviewing the AMA framework; and e. Changes that cause a considerable alteration to the operational risk capital charge. The alteration should be calculated by comparing the capital figure resulting from the application of the actual AMA model and the proposed model after the changes. If the AMA is applied on a unified basis, the alteration is to be calculated only at group level. Competent authorities may set a threshold to define what constitutes a considerable alteration. D) Minor changes to the AMA All changes which do not meet the criteria defined in the institutions AMA Change Policy under one of the previous categories (A-C) above and which do not fall under one of these categories even when considered in connection with other changes, according to point 4.2 above of the Guidelines, should be deemed to be minor changes to the AMA.
IV. Accompanying documents
a. Cost- Benefit Analysis / Impact Assessment
Costs and benefits regarding the Guidelines on AMA changes......................... 15
Costs and benefits for Institutions .............................................................. 15
Costs and benefits for competent authorities ............................................... 16
Impact on the economy ............................................................................ 17
Conclusion............................................................................................... 17
Costs and benefits regarding the Guidelines on AMA changes
The Guidelines harmonise practices and procedures for the internal practices
of institutions and for the supervisory treatment of extensions and changes to an Advanced Measurement Approach (‘AMA’) used for determining the regulatory capital charge for operational risk.
The number of AMA institutions within the EU is limited. However, the AMA
is mostly used on a group wide basis by larger banking groups, covering a significant part of the financial market.
The Guidelines deal only with the process for the approval of and
communication with competent authorities regarding AMA extensions and changes, aiming at the introduction of a common process throughout the EU. The Guidelines do not contain requirements regarding the modelling or risk management of institutions. Therefore costs for changes to the model or the approval of such changes are not triggered by the Guidelines. Costs and benefits for Institutions
To comply with these Guidelines, institutions need to develop an internal
AMA change policy in line with the Guidelines. In particular institutions need to develop internal criteria to map possible changes to the categories defining the materiality of the change.
AMA institutions must comply with the regulatory requirements at all times.
For this reason, institutions should already have in place an internal policy on how AMA changes are approved internally as part of their AMA framework. Such existing processes and the respective documentation need only to be amended and extended as a result of the need to comply with these Guidelines.
Similarly, institutions already need to review and update their internal
policies asa regular task. It can be assumed that the amendment of internal AMA policies can be achieved by the staff in place within the operational risk management function. Therefore the development of the internal AMA change policy should only cause limited one off costs in the form of time commitment by existing staff and time commitment to maintain the policy.
Finally, institutions need to communicate AMA changes to the competent
authority. The Guidelines clarify the communication requirements and the range of changes, which require a new approval. Clear processes reduce the costs of communication with competent authorities and provide more legal certainty regarding AMA changes. Costs and benefits for competent authorities
The Guidelines should be implemented by national competent authorities in
their national rulebooks. Competent authorities will receive the institutions’ internal AMA change policy and will have to conduct change processes in line with the procedures set out in the Guidelines.
The implementation of the Guidelines on AMA changes will trigger one off
costs for amending supervisory rulebooks and internal documents. A limited number of staff members in charge of the supervision of AMA institutions or subsidiaries of AMA institutions need to be informed. 10.The Guidelines will trigger minor additional one off costs in the form of time commitment for the review of the internal AMA change policies submitted by institutions. Competent authorities in charge of the supervision of AMA institutions need to be informed about the institutions internal policies as they will be involved in the change processes later on. 11.Competent authorities have to deal with AMA change processes anyway; this is not triggered by the Guidelines - hence these Guidelines do not give rise to any cost for the actual AMA changes. On the other hand, they are expected to give rise to the following benefits: firstly, a harmonised process is expected to facilitate communication and coordination efforts regarding the involvement of host supervisors; Secondly, these Guidelines will help to ensure that the relevant competent authority is informed in a timely manner about changes to the AMA. 12.In some cases the Guidelines state that a change has to be approved. This is just a clarification of the existing article 105 of Directive 2006/48/EC and not a new regulation. The Guidelines provide an interpretation about when such an approval is needed. Approval processes are already in place and competent authorities need to review the AMA regularly. The Guidelines ensure a level playing field regarding the approval of AMA changes across the European Union. In addition they ensure a more efficient interaction between competent authorities and firms, as approval is only required for changes of higher materiality rather than for every change. 13.For the above reasons, the Guidelines on AMA changes are not expected to trigger significant costs. Instead, they are expected to give rise to additional benefits, such as the establishment of harmonised processes, which facilitate the coordination of supervisory tasks among supervisory authorities. These Guidelines may therefore increase the efficiency of banking supervision in the field of AMA institutions.
Impact on the economy
14.The implementation of the Guidelines is expected to improve the communication between competent authorities and institutions. The implementation costs themselves are very low, so that the Guidelines have no impact on the economy in general. As the Guidelines do not change the capital requirements, it is not expected that they have any impact on the lending capacity of the banking system or other services offered. 15.States outside the EU (e.g. other Members of the Basel Committee), which have implemented the Basel II framework, are also faced with applications of banks to change the models used for measuring the regulatory capital requirements. An AMA approval process is also required by the so called Basel II framework. The mere clarification of approval and communication procedures has no impact on the level playing field of EU-institutions compared to non EU– institutions. Conclusion 16.The implementation of the Guidelines is expected to trigger low one-off costs for AMA institutions and competent authorities. It is hoped, as a result of the implementation of the Guidelines, that clear communication rules will lead to a smoother process, avoiding case by case decisions on the appropriateness of a process and reduce the cost for home/host coordination of competent authorities regarding this matter. It is also expected that institutions will have more legal certainty about AMA changes being in line with supervisory requirements. An impact on the economy of the EU or a single member state is not expected. The costs arising out of the implementation of these Guidelines are not unreasonable, especially when compared to the expected benefits, i.e. the achievement, throughout the EU, of a more consistent treatment of AMA changes.
b. Feedback on the public consultation and on the opinion of the BSG
technical standards on the conditions for assessing the materiality of extensions and changes to the AMA will be developed.
7. A detailed account of the comments received and the EBA´s responses
to them is provided in the feedback table below. Final minor drafting changes, in particular in the introduction section of the Guidelines, have been made in order to adapt these Guidelines to the EBA style guide. Those amendments do not change the content of the Guidelines, and have thus not been mentioned in the feedback table.
Feedback table on CP 45: analysis of the responses and suggested amendments The first column of the feedback table makes reference to the terminology and paragraph numbering used in the original CP 45. The last column refers to the terminology and numbering in the final EBA guidelines. CP 45 Summary of comments received The EBA’s response Amendments to the proposals Guidelines on AMA Changes General Comments The Guideline has been restructured to comply with the quality criteria for EBA guidelines. As a result, the numbering of paragraphs has changed and a executive summary has been added. The changes concern only the format and structure of the document however, but not its content. Respondents stressed that it is important to apply the principles in a way that is proportionate to the scale and complexity of businesses. The Guidelines apply to all institutions using an AMA, irrespective of their size and complexity. However, smaller institutions usually use one of the simpler approaches. The requirements take the No change
severity of an AMA change into consideration and define proportionate measures. Respondents pointed out that the consultation paper did not contain any guidelines on validation in a home-host context and on
Article 129 of Directive 2006/48/EC.
The Guidelines on Validation contain guidelines on validation and on home-host procedures. It is not intended to duplicate existing guidelines. Those Guidelines are published on the EBA website. No change
saw that the task could either be performed in the internal audit or internal validation function. conduct a review is of lesser importance, as long as the objective is achieved. This review is independent of internal audits performed in this area. amended 17 Respondents asked for clarification on whether a group-wide AMA change policy would be sufficient or whether subsidiaries were required to have individual AMA change policies. In the latter case, the question arises as to whether subsidiaries rolling out an AMA might have to provide that policy, possibly even before their parent groups have developed such a policy. In addition, clarification was requested regarding AMA changes in a situation where an AMA EU subsidiary has a non-EU parent institution. In this context respondents also required clarification about the implementation date and when such a policy needed to be in place. In an AMA group it would be sufficient to develop one, central, group AMA change policy. However, subsidiaries should have knowledge of the policy. Requests to extend or significantly change an AMA should be submitted by an EU parent credit institution or, jointly, by the subsidiaries of an EU parent financial holding company. The competent authorities will follow the procedures envisaged by
Article 129(2) of Directive 2006/48/EC.
The Capital Requirements Directive (CRD) applies to institutions within the EU. If an EU subsidiary of a non-EU parent intends to use an AMA, the institution (i.e., an EU-institution) or EU parent institution (i.e., the EU subsidiary or another EU subsidiary which is considered as the parent institution) will need to gain permission from the competent authorities. With respect to extensions and changes, the Guideline on AMA Changes will be applied accordingly to the AMA used for calculating the capital requirement for operational risk. The implementation date applies to the competent authorities. AMA institutions will be informed by the competent authorities. - Granting 6 months for Background Paragraph 8 and Article 5(1) amended
the development of a model change policy is considered appropriate.
3. Supervisory procedures for AMA extensions and changes
Chapter
3.1. and
3.2.
Respondents suggested setting a deadline for the responses of the competent authorities to the different categories of change and proposed that changes should be automatically considered as approved after the expiry of that deadline. Explicit approval is required for an AMA. The same applies to extensions and significant changes. As the severity of a change may be adjusted by the competent authorities, the suggested approach cannot be applied to any change. No change 21 Respondents suggested that the flow of information be specified, in particular in a home/host context. Foreign subsidiaries should communicate changes via their parent companies. Communication between the home/host competent authorities is dealt with in the Guidelines on Validation. The institution or, if the AMA is used on a unified basis (Article 105 of Directive 2006/48/EC), the EU parent credit institution or EU parent financial holding company, is responsible for communication with the competent authority. The scope of the Guidelines has been clarified. Background Paragraph 8 and Article 5(1) amended 21 Respondents suggested stressing that the approval process was coordinated by the consolidating supervisor. The consolidating supervisor should align all supervisors in a College of Supervisors, including a key role for the EBA. Communication between the home/host competent authorities is dealt with in Article 129 of Directive 2006/48/EC and the CEBS Guidelines on Validation. The responsibility for organising and coordinating the approval process for extensions and significant changes to an AMA lies with the consolidating supervisor. This has been clarified. Background Paragraph 8 amended and explanatory note to Article 5(1) added
23 Respondents suggested that institutions should mandatorily provide an independent review as per the ‘extensions’ and ‘significant’ categories for major changes as well. The review should be proportionate to the severity of a change. Also, with respect to major changes, the review should be led by the consolidating supervisor, with further reporting in the College of Supervisors, including a key role for the EBA. If major changes are reclassified into a more severe category, the respective documentation requirements will apply. Institutions are required to perform regular reviews of their AMAs, thus an additional mandatory review before the implementation of a major change was considered to be too burdensome. No change 27 Respondents asked for confirmation, by stating as an example, that notification of minor changes could be carried out by inclusion in the annual AMA assessment. The Guidelines set out a minimum requirement for the reporting of minor changes to the competent authorities. Institutions need to comply with the national implementation of this Guideline, which may comprise a higher reporting frequency. No change
Annex
General
Comment
The Annex should specify that it relates primarily to material changes to AMA policy/methodology. The term ‘methodology’ better reflects the underlying principles of internal loss data collection; procedures normally relate to internal activities that may change frequently without impacting the principles of loss data collection. Notifying the regulator of procedural changes would probably cause a significant administrative burden, while Institutions need to comply with all requirements of Annex X, Part 3 of Directive 2006/48/EC. This contains the loss data collection. As a change of process might also impact on the quality of data or, in other cases, the use of an AMA within risk management procedures (e.g. the use test) such changes cannot be excluded from the AMA change Guidelines. No change
providing little insight into bank policies.
General comment
The Annex contains examples which could be further clarified. E.g., ‘Changes that cause a relevant alteration to the operational risk capital charge’. One Respondent suggested ‘that ‘relevant’ could be clarified by setting a specific threshold of 5 %. Other respondents asked for guidance on what a material alteration of the capital charge was. Participants in the public hearing suggested developing more concrete quantitative criteria to distinguish between major changes and significant changes. This could be done via percentages of capital changes or by comparing the statistical uncertainty of a model before and after a change. To avoid smaller changes adding up to a significant change without supervisory involvement, the most recent approved model would need to be maintained. A more specific technical instruction on how to calculate those thresholds would be needed. Both would create an additional burden for institutions and supervisors. The implementation of this aspect will be reviewed by the EBA and taken into account when binding technical standards on the conditions for assessing the materiality of extensions and changes to the AMA will be developed. No change General comment Respondents stated that the definitions in the
Annex were contradictory to some extent, as
named examples should be treated as stated in the Guideline, but changes which would alter capital relevantly needed to be assigned to the major changes category. In some cases the categorisation of a change might be controversial, as the actual quantitative impact and the categorisation based on the kind of change may be different. In such cases institutions should choose the more severe category.
Article 4(4)
added.
General
Comment
One respondent was of the opinion that the categorisation of the types of AMA changes was overly complex and suggested that institutions should define their policies. The Guidelines contain four categories, with as well a reasoned differentiation of the communication, notification and approval requirements. The procedures themselves only consist of three categories, as the procedures for AMA extensions and changes are identical, while the kind of change is different. With an AMA extension, a new and not yet approved element is implemented or the scope of a partial use is extended beyond a previously agreed roll-out plan. On the other hand, AMA changes amend already approved AMA elements. The Guidelines differentiate between significant changes which need prior approval and major and minor changes, neither of which requires a formal approval process. However, differentiation is needed to avoid situations where a lot of minor changes are only notified after one year. Those changes could, considered together, be significant. Therefore the category major changes was introduced, to ensure timely notification and assessment of changes, enabling the competent authorities to decide whether prior approval would be needed. This closer cooperation between institutions and competent authorities will help to create a better understanding of the scope of changes which are acceptable without prior approval or which require prior approval. This improved understanding is needed in order to develop criteria for the assessment of the severity No change
of model changes, which will lead to a more stringent categorisation of AMA changes. The Guidelines require institutions to define their model change policies in line with the guidance provided. To ensure fair treatment and a level playing field, common procedures need to be established. A and B It was suggested that the categories in the
Annex be aligned more with the chapters of the
Guidelines by merging Sections A and B.
As the document has been restructured, the categories have been kept separated in the Annex. No change
Annex, A,
st bullet
It was suggested that the significance of the extensions to the scope of the AMA framework (and the distinction between EU and non-EU extensions) being taken into consideration. Within the calculation of the capital requirement for operational risk, institutions need to take into account mergers and acquisitions and changes of internal business structures. This may also impact on the scope of an AMA. If such extensions or changes only have an insignificant influence on risk profiles, institutions may apply such changes without a prior approval process and include those changes in the major and/or minor changes category. A footnote has been added.
Annex, A, 2 a
amended
Annex, B,
th bullet
Respondents asked to clarify which changes were considered to be fundamental, e.g., those which would impinge on the independence of the operational risk management function. The comment has been accommodated and examples added.
Annex, B, d
amended
Annex, C,
nd bullet
The example has been clarified. Annex, C, b amended
Annex, C,
rd bullet
It was suggested that the word ‘fundamental’ be changed, as this was also used within the examples under B, ‘significant changes’. The wording was changed to ‘relevant’. Annex, C, c amended
Annex, C,
th bullet
It was suggested that the example regarding validation be clarified. Validation is a broad concept. In this bullet point the changes should refer to changes within the logic and methods used. The comment has been accommodated. Annex, C, d amended`
Annex, D The category ‘Minor Changes’ have been added to
the Annex, to provide definitions for all 4 categories.
Annex, D added
V. Form for Confirmation, on the part of
Competent Authorities, of Compliance with these Guidelines
Confirmation of compliance with guidelines and recommendations Date:
Member/EFTA State:
Competent authority:
Guidelines/recommendations:
Name:
Position:
Telephone number:
Email address:
I am authorised to confirm compliance with the guidelines and recommendations on behalf of my competent authority: Yes The competent authority complies or intends to comply with the guidelines and recommendations:
Yes No Partial compliance
My competent authority does not, and does not intend to, comply with the guidelines and recommendations for the following reasons :
Details of the partial compliance and reasoning [TBC]:
Please send this notification to compliance@eba.europa.eu.
In cases of partial compliance, please include the extent of compliance and of non-compliance and provide the reasons for non-compliance for the respective areas. 6 Please note that other methods of communication of this confirmation of compliance, such as, communication to a different e-mail address from the above, or by e-mail that does not contain the required form, shall not be accepted as valid.
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