Sterling Medical Devices, a fully staffed U.S. based medical device engineering firm, is entirely dedicated to helping our clients resolve medical device development process challenges – from concept through completion – by applying our expertise of almost 20 years in the industry. We address the whole development process: systems, software, electronics, mechanical, quality, and compliance.
Our staff consists of teams of medical device trained experts and certified project managers, working exclusively on projects in the medical Device industry. We incorporate the most current FDA guidelines and regulations, best practices and latest tools in the industry for your development projects – or any parts of it, based on your company’s specific needs. We can help you optimize your budget and shorten development times for your Class l, ll, or lll device through the use of the latest tools and technologies. If you have a technical issue or other problem that is delaying your current project, we have the resources and expertise to jump right in and get your project back on track. Our approach allows our clients to get to market faster, streamlines the regulatory process, minimizes risk and saves cost.
Unlike some of our competitors, we do not have a stake in the manufacturing revenue stream, so we do not reuse work that is not optimized for the product simply to move more quickly to the manufacturing phase, leaving you to defend design risk challenges to your product. We adhere to budget and schedule while designing our clients’ products with a focus on user needs, requirements, all the while making smart design choices based on our extensive and diverse product development experience.
Helping you meet regulatory goals
Sterling Medical Devices is ISO13485 registered, IEC 62304 compliant as well as ISO 14971 and IEC 60601-1 compliant, so the work product we produce for our clients is consistent with the highest industry standards. Don’t yet have a quality system? You can rely on ours while in the process of achieving your own. Or, if you prefer, we can work with your team to develop your own quality system in a cost effective manner. Our clients often leverage our ISO certified QMS, IT infrastructure, and experience.
Maximizing efficiency through experience and state of the art Tools and equipment
Sterling owns and licenses the most up to date and advanced state-of-the-art tools and validated equipment and employs it on its clients’ projects so they can benefit from increased accuracy, efficiency and latest technology applied in tools. Sterling also offers its clients extensive IT infrastructure and real time backups of their work that is also transparent to them in real time. We own leading edge collaboration tools and use them in house.
Sterling offers the following advantages to its client:
• U.S. Based Full Time Engineering Staff
• Validated Tools, Staff Trained
• Experts in Regulatory Concerns
• Extensive IT Infrastructure/Real-time Backup
• Leading edge collaboration tools » Polarion and Skype for Business
• Engineering/Design Focused with Design for Manufacturability
• Transparent, Customer Focused
• Next Generation Project Management
• Work with companies from startups to the well established
» Startups leverage our ISO certified QMS, IT infrastructure, and experience
» The well established utilize our talent and expertise to get the job done right
ISO 13485 Certification – ISO 13485 is an internationally recognized quality standard for the medical device design, development, production, and the sale of medical devices. To be certified, organizations must demonstrate an ability to provide medical devices and related services that consistently meet customer and regulatory requirements. In addition to approving Sterling’s quality systems and practices, ISO certification allows our customers to streamline their auditing process.
As a forerunner in custom software solutions for the medical device development industry, Sterling Medical Devices is affiliated with the leading industry associations.