Академический Документы
Профессиональный Документы
Культура Документы
1.0
Description
New Check List adapted from CMMI
guidelines and Raytheon Systems
Engineering practices by Ken Jensen
(Raytheon Information Solutions). Initial
version named T-11.1.
Revised Sheets
N/A
2.0
3.0
Check List
Date
October 1, 2009
Disposition (Conditional Pass) - Fill in an "X" if the item receives a "Conditional Pass" disposition.
Disposition (N/A) - Fill in an "X" if the item receives a "Not Applicable" disposition.
Risk - Provide a risk evaluation. Standard evaluations are comprised of four levels (High, Medium, Low,
None). It is recommended that the cells be filled in with (Red, Yellow, Green, Blue) fill color corresponding
to the risk level.
Action (Y/N) - Fill in "Y" if there is at least one open action associated with this item; if no actions, fill in "N".
An item with a risk evaluation of Medium or worse should generate at least one action. Low risk items may
also generate actions, at the discretion of the reviewers.
Comments - Include any explanatory comments (e.g. rationales for the disposition of the item, rationales
for the risk evaluation, description of open actions, identification of the review that should address the
actions).
Each item should have an "X" filled in for one, and only one, of columns C, D, E, F or G
Detailed instructions for filling in the checklist can be found in the STAR EPL Process Asset "Critical
Design Review Peer Review Guidelines" (PRG-8.1)
Disposition
CLI #
1.0
Introduction
1.1.1
1.2.1
1.3.1
1.3.2
1.3.3
1.4.1
1.4.2
1.5.1
1.6.1
1.7.1
1.8.1
1.9.1
2.0
PDR Report
2.1.1
2.2.1
CDR entry criteria are listed completely and correctly in the CDD
2.2.2
2.2.3
2.2.4
2.2.5
2.2.6
Pass
Conditional
Pass
Defer
Waive
N/A
Risk
Action
(Y/N)
2.2.7
2.2.8
2.2.9
2.2.10
2.2.11
2.2.12
2.2.13
2.2.14
2.3.1
CDR exit criteria are listed completely and correctly in the CDD
2.3.2
2.3.3
2.3.4
Deviations from CDR exit criteria that were established at the PDR
are approved and documented in the CDRR.
3.0
Operations Concept
3.1.1
3.1.2
3.2.1
The CDD and OCD satisfactorily explain why the products are
being produced.
3.3.1
The CDD and OCD satisfactorily explain how the products will be
used.
3.4.1
The CDD and OCD satisfactorily explain how the products should
be produced. Production and delivery scenarios have been
described, consistent with the level of detail in the customer's
concept of operations and the production environment constraints.
4.0
Requirements
4.1.1
4.2.1
4.3.1
4.3.2
The CDD explains the rationale for each new requirement since
PDR, notes the potential effects on the project plan, documents
the agreement of affected stakeholders, notes new or modified
risks that result from the new requirement and notes any
recommended actions that result from the new requirement
4.4.1
4.4.2
5.0
5.1.1
5.2.1
5.2.2
The algorithm objectives are derived from and consistent with the
operations concept
5.3.1
The attributes of the sensing system(s) used to supply data for the
algorithm are described in the CDD and ATBD.
5.3.2
5.3.3
5.4.1
5.5.1
5.6.1
5.7.1
5.7.2
5.8.1
5.9.1
5.10.1
5.10.2
5.10.3
5.10.4
5.11.1
6.0
6.1.1
6.1.2
6.1.3
6.2.1
6.2.2
The required criteria for external interfaces are listed in the CDD.
Deviations from the STAR standard criteria are noted and
explained.
6.2.3
6.2.4
6.2.5
6.3.1
6.3.2
6.4.1
6.5.1
7.0
7.1.1
7.2.1
7.2.2
7.3.1
The detailed design for each unit fully defines the structure and
capabilities of the software product components at the Unit-Layer
7.3.2
The detailed design for each unit, fully defines the structure and
capabilities of the software product components at the Sub-UnitLayer
7.4.1
The detailed design for each unit, fully describes each Look Up
Table (LUT) in the algorithm design
7.5.1
The detailed design for each unit, fully describes all parameter
files, system control files, input/intermediate/output data files, and
ancillary data files in the algorithm design
7.4.1
The detailed design for each unit, fully describes each Look Up
Table (LUT) in the algorithm design
7.5.1
The detailed design for each unit, fully describes all parameter
files, system control files, input/intermediate/output data files, and
ancillary data files in the algorithm design
8.0
Quality Assurance
8.1.1
8.2.1
8.2.2
8.2.3
The CDD describes the CM/DM tools that are in use for the project
8.2.4
8.3.1
8.3.2
8.4.1
The CDD, VVP and DPP consistently identify the work products to
be verified and the requirements to be satisfied by each work
product selected for verification.
8.4.2
8.4.3
8.5.1
8.5.2
8.5.3
8.5.4
The CDD and VVP identify the tools and training available for
Operations and Maintenance (O&M).
8.5.5
The CDD and VVP describe the scope of the validation for each
operator need.
8.5.6
The CDD and VVP identify user needs (training, support, use of
products) to be validated.
8.5.7
The CDD and VVP identify the tools, training, and support
services available to the user, and the procedure for delivering
these to the intended users.
8.5.8
The CDD and VVP describe the scope of the validation for each
user need.
9.0
Requirements Allocation
9.1.1
9.2.1
9.2.2
9.2.3
10.0
10.1.1
10.1.2
The CDD reports the status of all PDR actions with sufficient detail
to allow the CDR reviewers to assess the current status of the
actions and their associated risks.
10.2.1
The CDD reports, in sufficient detail, the status of each risk that
has been identified since PDR.
10.2.2
The CDD reports the status of all new actions with sufficient detail
to allow the CDR reviewers to assess the current status of the
actions and their associated risks.
10.3.1
10.3.2
10.3.3
11.0
11.1.1
11.2.1
11.3.1
The CDD lists all outstanding issues, actions and risks that require
attention.
The CDD lists the recommendations of the development team for
the next steps after the CDR.
Comments