Each client determines the scope of our involvement based on the complexity of the project, or the size and skill set of the client’s own staff. Following is a brief overview of our services:
An effective software process is essential for creating high quality medical and laboratory products. Therefore, one of the first steps of the project is to meet with your staff to determine details of the software process -- selecting tools, determining how reviews will be handled, and deciding on the approach to configuration management and testing. While Syncro Medical has a well defined software development process of its own which can be used for the project, many clients ask that we adapt to their process, which we are happy to do. The approach to documentation will be planned as well during this early stage. Often, Syncro Medical uses the Unified Modeling Language (UML) to create and review design, and also to document the results for regulatory submission and ongoing support and maintenance. Successful software development begins with a clear understanding of product requirements. Syncro Medical engineers are available to work with your team to capture and document requirements. In many cases, we utilize Rapid Prototyping techniques to help our clients more quickly decide on workflow, screen layout, and general "look and feel". (In some cases, the prototype is used by the client's sales staff to begin pre-selling the product while development is underway.) Syncro Medical has extensive experience in
translating end-user requirements to underlying software requirements,
and then documenting them to
provide a solid framework for subsequent design, implementation and
test. Using such tools as Doors or Requisite Pro, Syncro initiates
the requirements traceability process during this step.
Working closely with the client, the Syncro Medical team develops a comprehensive Test Plan. Typically, test scripts are written during this stage and automated testing tools are utilized where appropriate. Depending on client preference, Syncro Medical can also support the project's Verification and Validation activities, beta testing, and phased roll-out. At Syncro Medical, we understand that correctly working software is only one element of a successful project. The quality of the documentation can be just as important for the success of your regulatory submission and for your ongoing support and maintenance of the product. Prior to hand-off, the complete documentation package, including requirements and design documents, source code, test plans and test results, is updated and prepared for final review and submission. |
||||
