Software Quality Assurance (SQA) for Small Business

 Software Quality Assurance Manual  


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

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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)