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 without doctors with experience in a particular field having an idea to develop a prototype medical device that could help patients, the future technologies that necessary to save lives are not achieved. But the long, arduous path through the FDA submission process to gain 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 five biggest mistakes medical device startups make when they go down that path. Here is the advice of Bruce Swope, VP Engineering, who has more than 25 years of management experience in medical device development, and Erik Hilliard, Director of Business Development, who has more than 25 years of management experience in medical device development. 10 years of working with customers to see their ideas come to market on how to avoid these mistakes and save money.

Contact Bruce or Erik for more information.
Visit: http://sterlingmedicaldevices.com/contact-us
Email: [email protected]
Call 201-227-7569 x2.

Please take the opportunity to connect and share this video with your friends and family if you find it helpful.