Are you looking to get your medical device project back on track? Our engineers are here to give you the advice and support you need at the right time. Questions to ask yourself about your specific project include:
Sterling Medical Devices is ISO 13485 certified and we work with medical device companies at any stage in their development lifecycle to ensure efficiency and bring your device to market.
With our familiarity of FDA regulations, Sterling helps relieve excessive regulatory burden by targeting specific aspects as valued by the industry. We have the experience and skills needed to quickly resolve your project development roadblocks.
Sterling Medical Devices has over 80 full time engineers on staff and the resources to take on any project you need assistance on. Check out our company overview page to learn more about our company.
Our engineers keep a constant level of communication not only with each other but with their clients as well using programs such as Polarion ALM to create a stress-free transparent environment.
We employ agile project management by breaking down the project into incremental steps, and then thoroughly reviewing each step. This allows us to efficiently make changes and receive company feedback. Check out our Risk Management page to learn more about how we mitigate risk and manage each project.
Sterling Medical Devices is equipped with different methods of medical device Tool Validation which gives our team the opportunity to see which methods fit best for you and your device.
February 18, 2021
September 8, 2020