DI-QCIC-81536A
Test Information Sheet (TIS)
The Test Information Sheet (TIS) is used to provide detailed planning information necessary to review the test program specifics, conduct the tests, record test data, and evaluate the test results.
Approval DateFebruary 27, 2018
AMSC NumberF9890
Preparing Activity11 (AFLCMC/WWM)
Project NumberQCIC-2015-012
OPR—
DTIC ApplicableNo
GIDEP ApplicableNo
Limitation—
Applicable Forms—
Approval Limitation—
Form Version—
DID Formatfree_text
963C CompliantYes
DISTRIBUTION STATEMENT A: Approved for public release; distribution is unlimited.
Application & Interrelationship
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Use & Relationship
The Test Information Sheet (TIS) is used to provide detailed planning information necessary to review the test program specifics, conduct the tests, record test data, and evaluate the test results.
a. This Data Item Description (DID) contains the format and content preparation instructions for the data product generated by the specific and discrete task requirement as delineated in the contract.
b. This DID is applicable to engineering (developmental), preliminary qualification, qualification, and acceptance testing.
c. This DID interrelates with DI-FACR-80810, Test Facility Requirements Document (TFRD).
d. This DID supersedes DI-QCIC-81536.
(Copies of these documents are available online at http://quicksearch.dla.mil.)
Preparation Instructions
1Reference documents.The applicable issue of the documents cited herein, including their approval dates and dates of any applicable amendments, notices, and revisions, shall be as specified in the contract.
2Format.Contractor format is acceptable.
3Content.The TIS shall include the title and number of the specification paragraph (if applicable), title of test, functional category, and whether flight or ground test. Each TIS shall include the following information, to the extent applicable on the particular test:
3.1The prioritized objectives, test conditions, success and failure criteria for each objective, and the step-by-step procedures to be followed.These procedures will be to the level of detail to allow reproducibility of testing.
3.2A description of each test item configuration as it relates to the system requirements, specification, and to the particular test.Examples of information include:
3.2.1The number of items to be tested and the number of times each item is to be tested.
3.2.2Description of all systems, subsystems, components, and their performance features having a direct bearing on the purpose of the test.
3.2.3Test parameters (e.g., velocity, altitude, flight maneuvers, power settings, weight changes, and center of gravity travel, etc.).
3.2.4Test profiles, performance predictions, anticipated system restrictions or limitations (redlines), with justification for each.Include specific high-risks to personnel and material or tests outside of normal parameters.
3.2.5Identification and location of all non-production equipment - data pickups, console controls, and recording equipment.For all non-production equipment used to simulate or substitute for production equipment (e.g., cables, etc.), identify the difference in salient characteristics (e.g., shielding, size, etc.).
3.2.6Test apparatus descriptions and method of installation.
3.2.7Safety considerations and hazardous operating procedures (e.g., propellant, electrical, high pressure, etc.).
3.2.8Security, including special access considerations.
3.3Test location(s), schedule, phasing, and duration of tests.
3.4Description of support equipment required from other sources, such as government furnished equipment or associated contractor equipment.
3.5Extent of government, prime contractor, and associated contractor participation.
3.6Type, number and description of data recording devices to be used.
3.7Data to be recorded, data reduction and analysis procedures, and data uncertainty criteria.Include test results presented in terms which can be correlated with specification requirements.
3.8Toxic materials used in or resulting from the test and their respective handling and disposal requirements and procedures.
3.9Proper location of warnings, cautions, and notes in the test procedures.
3.10Certification(s) for personnel operating facility equipment.
3.11Recovery methodology in the event of test failure, including restart criteria (e.g., start over, start at last step successfully completed, etc.).
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