How Regulatory Changes Can Impact Product Development

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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.

Resources

Man conducting third party compliance audit.

February 2, 2023

Uncovering the Benefits of Third-Party Compliance Auditing

The importance of maintaining a high level of quality and compliance can’t be overstated for medical device companies. Failing to do so can put patients at risk, land you in hot water with...

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 Helps Print Parts Win Contract with City of New York for Production of Medical-Grade Nasal Swabs

Sterling Medical Devices performed design services for a Class III breathing pacemaker with Major Level of Concern software, intended for use by patients who have lost neurological control of respiration. This life-sustaining device is comprised of two main components: an internal passive receiver and an external controller....

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!

How Regulatory Changes Can Impact Product Development