Syncro Medical
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. Competition within the medical device industry continues to intensify. Increasingly, it is the medical device software component that provides the primary aspect of product differentiation in the marketplace. In order to increase R&D bandwidth and to speed new products and enhancements to market, leading manufacturers are routinely employing software development outsourcing. Because of this, choosing the right software development partner is a critical business decision – one that can have far-reaching consequences. Syncro is joining leading companies across multiple global industries in committing to net zero carbon emissions by 2040 to accelerate the transition to a lower carbon economy.
Company details
Find locations served, office locations
- Business Type:
- Manufacturer
- Industry Type:
- Medical Equipment
- Market Focus:
- Globally (various continents)
About us
A Leader Among Medical Software Companies
As a pioneer in outsourced software development in the early 1980s, Syncro Medical’s founder, Dale Van Aken, refined a model for successfully providing medical software development to medical device manufacturers. Today, almost 40 years later, we continue to combine deep medical device development experience with a culture that values craftsmanship, expertise and integrity to ensure that our clients deliver industry-leading products to the market.
Syncro Medical has consistently maintained an outstanding reputation in the industry. Across 400+ projects, nearly 100% of our clients strongly agree that Syncro Medical provides significant value to their business. Our flexible, collaborative approach to software project management ensures that our clients achieve not only fast time-to-market but superior product functionality, quality and scalability as well.
Medical Device Software Standards
As an ISO 13485/9001 certified organization we ensure that your product meets both software standards and FDA medical device regulations for approval.
We’re honored to put our stamp of quality on so many category-leading products. Bring us your most difficult medical device product development challenges that will engage our passionate and uncommonly gifted team of developers. We’ll respond with a wealth of experience and a perspective that ensures outstanding results that exceed medical device standards.
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.
Our Core Values
We believe that the client’s trust must be earned by striving to understand the client company DNA and truly seeing the development needs through the client’s eyes.
What we Offer Our Clients
Syncro Medical’s strongest and most valued asset is its exceptionally capable and deeply experienced Engineering team. A typical engineer has been developing medical product software for nearly 15 years. Each Agile Certified team brings a wealth of perspective, talent and experience to every client engagement, resulting in rapid spin-up and efficient execution. Standing behind them is our Quality team with its integral management and FDA compliant process.
Our Engineering Managers are seasoned professionals in both software engineering and project management. Each has many years of experience assembling project teams, understanding client needs, and planning and executing medical development projects.
Over the years, we have learned what’s required to provide superior results. It starts with having a Syncro Medical team that thoroughly understands your requirements, including the nuances that can easily be lost in translation. When critical project communication needs arise, we’re at most a couple of time-zones away.
Because our entire engineering operation is here in the US, we can easily be at your site when required for crucial stages of the development process.
The Syncro Medical Development Center is located north of Philadelphia adjacent to Interstate 95.
Syncro Medical’s Agile development practice ensures the optimal mix of productivity, flexibility, and quality. Our certified Scrum Masters continually refine our process to effectively define and manage user stories, to work closely on sprint planning and task burndown, and to demonstrate sprint completions.
Syncro Medical clients see a new increment at each sprint review. This occurs at the project sprint interval, commonly every 3 weeks. The sprint cycle gives clients the opportunity to test and inspect the product frequently throughout the development process, and to have it on hand for demos. This feedback cycle helps ensure compliance and correctness of the software, and offers the client unlimited opportunity to revise operational features.
Working with Syncro Medical
Over 30+ years, Syncro Medical has completed many hundreds of software projects, earning the trust and confidence of scores of medical manufacturers from startups to major internationals. We’re honored to put our stamp of quality on so many category-leading products. In virtually every case, our clients ask us back to contribute again – for a new development phase or for an entirely new product. Bring us your interesting, industry-leading product development challenges that will engage our team of uncommonly gifted developers. We’ll respond with a wealth of experience and a perspective that ensures outstanding results. Period.