Software Quality Assurance (SQA) for Small
Business
Software Quality
Assurance Manual
Training
Small
companies often achieve poor results with software development projects.
Typical
problems are:
·
Cost
overruns
·
Schedule
delays
·
Product
or process performance deficiencies
What
is required is a commitment to an effective software development
process, which includes configuration management, training, and support
to make it effective in your company. We
have developed a software quality assurance system, which is
easily customized for small businesses.
We have eliminated the bureaucratic
approach commonly found in many large companies. Our software
quality assurance system is sensible and flexible and an excellent fit
in today's continuously changing business environment.
When
you install our
documented ISO 9001 and
ISO 26000 compliant system in your organization, you will
be
able to gain control of your software development process, quickly and
at a reasonable cost. You will receive a sensible and
flexible quality
manual,
23 associated procedures and 37
forms/templates which, when implemented in your
business, will significantly strengthen your software development
process (including hardware). You will find that your
defect rates and costs are reduced to a minimum, and follow-up
time will be minimal.
View
software quality assurance sample manual
Order
software quality assurance manual
Quality
Manual for Medical Device Software
If
you are a manufacturer of medical devices which
includes software, or where the software is the actual medical device,
our ISO
13485 Quality Manual for Medical Device Software will meet
your needs. This manual complies with ISO
13485:2016 and IEC 62304:2006. It
includes 25
procedures, and 42
forms/checklists which you customize specifically for your
needs. You
will receive sensible/flexible procedures which, when implemented, will
reduce
paperwork to a minimum and will enable you to significantly improve the
quality
of your products/services. This
documentation also complies with the
FDA’s CFR
21 Part 820:
Quality System Regulation.
Order Quality Manual (Item #23)
Training
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