For all of these projects, Syncro Medical's considerable experience with 510(k), PMA, or CLIA submissions has ensured a successful outcome for our clients. We understand regulatory process requirements. And we're comfortable with the software tools used for traceability, code documentation, and testing. As a result, your software will be submission-ready.
Our Knowledgeable Staff
As a successful service firm, Syncro Medical's staff is its core asset. We set a very high bar in the hiring process and then work hard to retain our quality staff, keeping them at the leading edge of software development technologies. As a result, we provide our clients with an engineering team that has exceptional capabilities and substantial experience developing medical products.
All of our engineers are degreed in Electrical Engineering, Computer Science, or Biomedical Engineering. Many have advanced degrees in these disciplines. In addition, Syncro Medical's typical software engineer has nearly 15 years of real-world software engineering experience -- much of it related to development of medical, laboratory and scientific products.
Given the caliber of our staff, and the fact that they have worked together as a development team on prior projects, we quickly spin up on new projects and then provide sustained high levels of productivity. Because we have exceptionally low turnover, our clients benefit from the continuity and our accrued knowledge of their products when engaging us for subsequent projects.
Importantly, Syncro Medical’s engineers are easy to work with. We understand the importance of functioning as a part of your team and fitting in well with your own staff.