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http://sterlingmedicaldevices.com How can medical device startups avoid costly mistakes when navigating the FDA submission process to successfully bring their idea to market? 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. Here are the 5 biggest mistakes medical device startups make when going down that road and advice from Bruce Swope, VP of Engineering, who has over 25 years' management experience in medical device development, and Erik Hilliard, Director of Business Development, who has over 10 years working with clients to see their ideas come to market, on how to avoid these mistakes and save money. Contact Bruce or Erik to learn more. Visit: http://sterlingmedicaldevices.com/con... Email: info@sterlingmedicaldevices.com Call 201-227-7569 x2.

http://sterlingmedicaldevices.com How much trouble and effort will it take to get FDA and CE Approval for my medical device? Regulators want to see a very specific design process, strong quality control, robust risk management and an airtight submission package. At Sterling Medical Devices, the FDA has accepted our thorough Design History Files (DHF) every time, showing that we have tried to think of every possible scenario through software verification and medical device testing. We ensure that the medical device software and medical device hardware are doing what they are supposed to be doing and designed to do. Learn more from Bruce Swope, VP of Engineering, who has over 25 years' management experience in medical device development, and John Campbell, Director of Quality, who has over 20 years in medical device development, device testing and verification. Contact Bruce to learn more. Visit: http://sterlingmedicaldevices.com/con... Email: info@sterlingmedicaldevices.com Call 201-227-7569 x2.