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Evidence Product Checklist for ISO/IEC 12207:2017 ''System and Software Engineering - Software Life Cycle Processes''
Abstract: Available
Author: Andy Coster CQI and Stan Magee CCP (Ret.)
Cover: Available
Customer Set for this product: Software and system engineering firms any firms that have a large complex software system
Format: PDF (Click here for our easy-to-modify Word® formatted version)
ISBN Numbers: 978-0-9770309-0-3
Language: English
Page count: 385
Provider: SEPT
Sample Pages: Available
Shipping: Available for download - Link will be provided in My ComplianceOnline section
Author: Andy Coster CQI and Stan Magee CCP (Ret.)
Cover: Available
Customer Set for this product: Software and system engineering firms any firms that have a large complex software system
Format: PDF (Click here for our easy-to-modify Word® formatted version)
ISBN Numbers: 978-0-9770309-0-3
Language: English
Page count: 385
Provider: SEPT
Sample Pages: Available
Shipping: Available for download - Link will be provided in My ComplianceOnline section
Price:
$167.00
Product Details
ISO/IEC 12207:2017 “System and Software Engineering - Software Life Cycle Processes” is often confusing and laborious. This is because directions contained in the standard can seem unclear or ambiguous therefore the experts at SEPT have produced a checklist. This checklist was prepared by analyzing each clause in ISO/IEC 12207 for key words that signify a required policy, procedure, plan, record, document, audit, or review. The resulting checklist then provides an easy-to-use categorized list of physical evidence against which you can audit your work products to help insure conformance with ISO/IEC 12207
To better understand this model a user of this product should understand SEPT definition of an auditor. An auditor can be your boss, an inside auditor or an outside auditor such as the FDA, DoD or a prime contractor for your product. The checklist will give the auditor and you a common reference point in the standard (Clause number) that becomes the index point for physical evidence. If a standard calls out physical evidence more than once , such as a “training plan” it is always index to the first clause that reference the training plan This method will allow you to organize you physical evidence in a systematic manner for presentation to the auditor. This simple checklist allows you to bring the document down to simple terms that a professional lay person can understand (policy, procedure, plans, records, documents, audits and reviews).
The checklist will allow the organization to divide the compliance activity into manageable work packages such as procedures, plans, documents etc.
The checklist is available in PDF or word format. The latter format allows you to tailor the document to your business case or the media that your organization wants to use the checklist in such as excel web page format or any other end product type in order to meet compliance with the standard in the most efficient way possible.
The checklist comes with 4 hours of free consultation, from experts that have firsthand knowledge of the underlying standard, to answer questions on the standards and checklists and is valid for 60 days after purchase of the product.
This product supports these Software Engineering processes
- Acquisition
- Code and Test
- Configuration Management
- Design
- Documentation
- Integration
- Life Cycle
- Maintenance And Operation
- Metrics
- Process Improvements
- Project Management
- Quality
- Requirements Definition
- Safety
- Security
- Verification And Validation
- Vocabulary
Customers of this product:
- AENOR, Span
- Alto Web
- Argonne National Laboratory - Library Acquisitions
- ASM Research, Inc
- ATK Thiokol
- Atos Origin, Belgium
- Berry Engineering
- Boeing
- BRIS, China
- Broker BioSpin Corporation
- Canadian Space Agency
- Capintec
- Cargo Logistics Corporation
- CCR Cost Recovery Services
- Comclin
- Concept Analysis and Integration
- Croatia Control Ltd
- Csgdelivers
- Datascope Corp, IPD
- Davis + Henderson, Canada
- Defense Manpower Data Center
- Draper Laboratory
- Ennovia, France
- Entergy Nuclear
- Faicorp
- Federal Equipment Company
- Gd-Ais
- Gdls-California Technical Center
- Ge Inspection Technologies
- Gm Defense - Delco Systems
- Gordian Solutions, Inc.
- Gwdi
- Helios Technology Ltd, UK
- IDR Inc.
- Impulse NC Inc
- Information Systems Laboratories
- Innermed
- Inner space Systems Corp
- ITT
- ITT Industries
- Knfcon
- Korea Railroad Research Institute
- Laird
- Lcontact9000
- Lorien Consulting, Finland
- Lumina Engineering
- M&M Precision Systems
- Maximum Technology Corporation
- Merck & Co., Inc.
- Meta-Fleet
- Navy Warfare Systems Agency
- Network Resources, Inc.
- Omnigon
- Pacific Consolidated Industries, Limited
- Paradise-Tech, Abu Dhabi
- Peterson Air force Base
- Phenomenome Discoveries Inc.
- Sensytech, Inc.
- Shinogi Qualicaps S.A., Spain
- Smsocs
- State Of Montana
- Systems-Enginuity
- T&T System, Italy
- Ta Tong Book Company Ltd, Taiwan
- Thales Information Systems
- Thirst
- Transas Marine International, Sweden
- Triumph Technology Inctaipie
- Tubitak Bilgem, Turkey
- Tubitak Uekae, Turkey
- UGL Limited Infrastructure, Australia
- Unites
- Unitrans’s, Israel
- Utanet, Australia
- Veridian
- Woodward Industrial Controls
- Xoran Technologies, Inc.
- Yakar Management Consultants Ltd, Israel
Note: “International Standards (ISO) define the best of practices for Medical Device and Software firms in producing a quality product. This checklist that SEPT produces will ensure that all of the best of practices are adhered to.”
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