ED Decision 2023/013/R
INSPECTIONS AND TESTS
Proposed type design: this term defines the type design (or the portion of the type design) as it is determined at the time when the testing and inspections are carried out.
Verification document (also known as ‘statement of conformity’): before each testing and inspection, the verification document must confirm that the test specimen conforms with the proposed design, the test and measuring equipment is adequate for the test, and the sensors and measuring system are appropriately calibrated.
Conformity of the test specimen: the documented verification is intended to ensure that the manufactured test specimen, even in the presence of non-conformities, adequately represents the proposed type design. Possible types of non-conformity may be the following:
— Non-conformity between the design of the test specimen and the proposed type design at the time of the test. These are typically identified in the early stage of the testing and inspection planning, and should be addressed as early as possible (e.g. in the test plan). There may be several reasons for such a non-conformity: to account for interfaces with the test equipment, to conservatively cover several or future design configurations, etc.
— Non-conformity between the manufactured test specimen and the design of the test specimen. Such a non-conformity may be the result of the manufacturing of the test specimen.
While it is convenient to define any possible non-conformity as early as possible, the applicant does not need to make the distinction between the two types of non-conformity above as long as they are explicitly addressed, justified in the verification document or by cross reference to the test plan or other documents. However, testing for the demonstration compliance with the applicable environmental protection requirements should be conducted in the final design of the product having incorporated the change.
Type certification is typically an iterative process in which the
design is under continuous evolution.
If the type design
evolves after the time of the testing and inspections, then the final
type design should be checked against the proposed type design (as it
was at the time of the testing and inspections), and the differences
(if any) should be analysed to ensure that the testing and inspection
results are representative of the final configuration. However, such
changes made to the type design may lead to the invalidation of the
testing and inspection results and the need to repeat the testing and
inspections. It is recommended that the design organisation should
have a thorough configuration management process to track the
evolving type design.
Conformity of test and measuring equipment: the configuration of the test and measuring equipment should be defined in the test plan and include the following:
— definition/design of the test equipment (relevant tools, mechanical parts, electronic components used to execute the test); and
— definition of the measuring equipment:
— type/model of sensors, together with their technical characteristics;
— position and orientation of exciters and sensors; and
— electronic measuring equipment (in some cases, this may also include the acquisition and post-processing of data).
The configuration of the test and measuring equipment should be defined and controlled through certification test plans and supporting documentation, according to the design assurance system, if applicable. The test plan should also include the following elements:
— the test cases, methods, and procedures for test execution;
— the pass–fail criteria; and
— pre-, during- and post-test inspections.
The verification document should confirm that the test and measuring equipment conforms to its purpose, and that the sensors and measuring system are appropriately calibrated. Any non-conformity should be assessed, and it should be justified that it will not compromise the test purpose and results. This may be done either in the verification document or by cross reference to other documents (test minutes of meetings, test notes, etc.).
Use of the term ‘adequate’: the test specimen, as well as the test and measuring equipment, is considered ‘adequate’ as long as the test execution on the manufactured test specimen (including any non-conformity) and the use of the installed test set-up do not compromise the test purpose and results (for example, by providing better performance than the proposed type design, or masking any potential failure mode or behaviour).
Changes that affect the validity of the verification document: if changes need to be introduced to the test specimen or to the test and measurement equipment after the verification is documented (and before the test is undertaken), then the verification document must be updated. The updated verification document must be made available to EASA before the test if EASA has informed the applicant that it will witness or carry out the tests or inspections.
Development versus certification tests: sometimes, tests of specimens that conform to a preliminary design, but are not intended for certification (known as development tests), are performed as part of a risk control strategy and to develop knowledge of a subject. Problems and failures found during development are part of the process of increasing the understanding of the design, including its failure modes and the potential for optimisation. Such development tests do not need to meet the requirements of point 21L.A.85(c).
Any planned test event should be classified in advance as either a development test or a certification test. Tests that support the compliance demonstration should be classified as certification tests.
It is acceptable for a development test to finally form part of the compliance demonstration, and it may be declared afterwards to be a certification test as long as it meets the requirements of point 21L.A.85(c). For this reason, it is important to keep the configuration of such tests under control.
If the test specimen used for a certification test has already undergone a series of previous tests that may affect or ultimately invalidate its acceptance as required by point 21L.A.85(c), this aspect should be considered when documenting the verification, and specific analyses or inspections may be required.
Because of the above aspects, EASA advises applicants to inform EASA if they intend to conduct a campaign of development tests that may eventually be used as certification tests to establish whether EASA would wish to witness the tests.
AMC1 21L.A.85(c) details conformity verification for test specimens and equipment, non-conformity handling, test plan content, and development vs certification test classification.
* Summary by Aviation.Bot - Always consult the original document for the most accurate information.
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