Sterling Medical Devices & RBC Medical Innovations are combining to create Vantage MedTech! Meet RBC
Contact Us
Close Form

Interested in learning more about how we can work together in your current or next medical device design project?

Just fill out this form and we’ll be in touch!

  • This field is for validation purposes and should be left unchanged.

Wherever you are in your product development lifecycle,
Sterling can help.

P: 201-877-5682
F: 201-301-9169

How Regulatory Changes Can Impact Product Development

How Regulatory Changes Can Impact Product Development: Insights from Global MedTech Regulatory Trends: True Quality Summit Series

The MedTech global regulatory landscape is evolving. What is the future of the medical device industry—and is your organization ready?

Regulatory and product development departments need to do more than cooperate—they need to work hand in hand. Hosted by Sterling Director of Regulatory and Clinical Affairs Carrie Hetrick, with other leading industry experts, this on-demand MedTech webinar offers best practices to help your team produce synergistic results.

Learn how a robust regulatory strategy can help you:

  • Establish a clear pathway to market
  • Make better and more informed decisions
  • Outline critical requirements to all development and business teams
  • Prevent delays, regulatory warnings, profit loss

The session is part of the digital MedTech conference, Global MedTech Regulatory Trends: True Quality Summit Series, presented by Greenlight Guru.

Watch How Regulatory Changes Can Impact Product Development now.

Contact Us

Share this!


United States of America and Medicine button on keyboard

March 17, 2022

What Country Leads the World in Medical Innovation

We’ll get right to the point. The answer to the question, “what country leads the world in medical innovation?” is the United States. Medical industry professionals all over the world...
Read More >
View More Blogs

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.
Read More >
View More Videos

July 12, 2022

Scalp Cooling System

Overview Paxman has been pioneering scalp cooling technology for over a quarter of a century. Paxman’s clinically proven cold cap technology has helped over 100,000 cancer patients in more than 60...
Read More >
View More Case Studies

Need help with your medical device?

Let Sterling Medical Devices show how to bring your idea from concept to prototype to
FDA/CE approval with a free custom project analysis.
Request Free Analysis