Wherever you are in your product development lifecycle,
Sterling can help.
Our knowledgeable and experienced team follows industry best practices in the process of the medical device software development lifecycle to ensure you develop a safe, effective, and FDA/IEC 62304-compliant product. We are ISO 13485-registered and -compliant and can help you align your medical device software development efforts with FDA expectations to help your project get to market faster. We offer services in mobile/app, cloud/web, firmware, and IoT development as well as cybersecurity expertise.
We have the expertise and skills you need to get your product to the market. Fill out the form below to get started.
February 18, 2021