Syncro Medical takes quality very seriously. We’re software craftsmen – attention to quality is part of our culture and embedded in every aspect of how we deliver our services.

Operating under the ISO process, our engineers understand the critical importance of documenting design, coding to a standard, and completing thorough unit testing and code reviews. All designs are approved by Syncro’s SEI-certified Director of Design and Architecture.

Syncro Medical is ISO 13485/9001 Certified. Whether you choose to use your Quality System or ours, we’ll provide the needed process and documentation for your FDA submission. Under the guidance of our Director of Quality, Syncro Medical’s fully independent QA engineers are an integral part of the team assigned to your project.

Safe, Secure & Reliable Software

for Your Regulated Medical Device


Syncro Medical’s QA Department consists of experienced software Quality Assurance engineers. The QA Engineers assigned to your project become an integral part of the development team, providing independent testing and verification of your product as the code is being implemented.


At the early stages of the project, Syncro Medical ensures that the architecture of your new product supports testability. For example, we’ll use an N-Tier architecture to decouple and abstract our functionality. Or we’ll incorporate design patterns, such as MVVM to further separate the presentation from the domain logic and allow for more thorough medical device software testing.


Each sprint cycle gives our QA team and our client the opportunity to run, inspect, and test the code throughout the development process. This client feedback cycle complements Syncro Medical’s testing effort, and thereby helps ensure compliance and correctness of the software.