Sterling Medical Devices & RBC Medical Innovations are combining to create Vantage MedTech! Meet RBC

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!

Name*
First Last
Email*
Phone*
Title
Company*
Message*
Phone
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
info@sterlingmedicaldevices.com

How Regulatory Changes Can Impact Product Development

Home > 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!

Resources

February 18, 2021

The New EU Medical Device Software Requirements

With the EU’s new medical device software (MDSW) requirements, the guidance related to qualification, classification, clinical evaluation and cybersecurity present challenges for software as a...

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.

Sterling Medical Devices Creates Controller to Groundbreaking New Multi-Pump Mechanical Circulatory Support Device

Controller to Power Groundbreaking New Multi-Pump Mechanical Circulatory Support Device Medical Device Need A controller for an implantable heart pump that...