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Bruce Swope

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Bruce Swope

Chief Commercial Officer

Chief Commercial Officer Bruce Swope has over 35 years of management experience in medical device software development, possessing exceptional knowledge of the medical device and software industries from both a business and technical perspective. In his role at Sterling, Mr. Swope is responsible for business strategy and development, including product development, service delivery, marketing, sales, and ensuring exceptional customer service. He has successfully managed software development teams of up to 150 people. Mr. Swope is an expert in leading Class III medical software products to commercial release. His depth of experience also spans the development of enterprise solutions, security applications, internal applications, and process control systems. Integral to these efforts has been his early adoption of quality practices including ISO 9000 processes, Common Criteria Certification, and Capability Maturity Model implementation. He earned his Bachelor of Science in Computer Science and Mathematics from the University of Louisiana Monroe. Mr. Swope finds value in seeing Sterling Medical Devices grow and the impact its work has made on improving and saving patient lives.

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Resources

medical device regulation compliance

October 22, 2021

Common Medical Device Regulatory Compliance Roadblocks

The medical device industry is heavily regulated by the FDA, specifically, the Center for Devices and Radiological Health. Unfortunately, while device manufacturers are required to establish and...
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February 18, 2021

5 Mistakes Medical Device Startups Make

Startups are the lifeblood of medical device innovation. Without universities researching ways to solve pressing healthcare problems or doctors with experience in a particular field who have an idea to develop a prototype medical device that could help patients, the future technologies needed to help save lives wouldn't happen. But the long, arduous road through the FDA submission process to get market approval can take a long time and cost a lot of money without help. Sterling Medical Devices has been helping startups through the FDA approval process since 1998 without ever having a submission rejected.
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Breathing-Pacemaker

September 8, 2020

Breathing Pacemaker

Sterling Medical Devices performed design services for a Class III breathing pacemaker with Major Level of Concern software, intended for use by patients who have lost neurological control of respiration. This life-sustaining device is comprised of two main components: an internal passive receiver and an external controller....
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