YOUR VISION REALIZED.

MEDICAL SOFTWARE DEVELOPMENT TO POWER ANY REGULATED MEDICAL DEVICE

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Medical Device Software Development
Regulated Medical Device Software Development
2018: Past Year Client Survey Results
FLEXIBILITY
PROJECT COMMUNICATION
PROFESSIONALISM
94%

strongly agree that Syncro Medical has superior technical knowledge

100%

agree that Syncro Medical provides significant value to their projects

95%

say that Syncro Medical meets cost targets

100%

strongly agree that Syncro Medical provides significant value

94%

felt in control of their projects

100%

strongly agree that Syncro Medical is highly responsive

Trusted By

Experts in Medical Device Product Development

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.

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.