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.
