Jamme Tan

Jamme Tan

Resource Director

Resource Director Jamme Tan has been a part of Sterling Medical Devices’ team for over 17 years, serving in multiple roles and advancing in company leadership. Mr. Tan has considerable experience in all phases of full lifecycle development under QSR compliant quality systems, especially with software and  project management using Agile practices. He leads Sterling’s team of software engineers and collaborates with clients to understand their project and needs, build an exceptional team, develop solutions to address their unique challenges, and bring their product to life. Mr. Tan has cultivated a broad expanse of expertise in software and firmware development utilized in crucial roles on project rescues as well as new product development across a broad range of projects, from wearable and implantable embedded systems to web portals and mobile applications. He earned his Bachelor of Science in Computer Engineering from New York University and is a Certified SCRUM Master and SCRUM Product Owner. Mr. Tan derives tremendous value from his work, improving processes and expanding the capacity of his team, secure in the knowledge that the state-of-the-art solutions he delivers offer remarkable benefits to Sterling’s clients and the people who need them. 

Resources

August 8, 2022

Medical Device Supply Chain

Medical Device Supply Chain Challenges and FDA Action Supply chain delays and disruptions can wreak havoc on any business, especially in the highly regulated medical device industry....
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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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