Watch the Video →

Interested in Greenlight Guru? See how we could help get your device to market faster, with less risk.

Get to Market

Sign up for free access:

By submitting your email you agree to the Terms of Service and Privacy Statement
Reserve your free ticket ➞

Whether you’re bringing your first device to market, or you have launched multiple already, our upcoming True Quality Summit Series is for you. There’s a variety of different topics designed to provide best practices for advancing throughout your product lifecycle and maintaining compliance across multiple markets.

Festivities kick off with a day dedicated exclusively to our customer community. From there, the True Quality Summit Series begins and anyone from anywhere can join, for free.

Proudly supported by

ABOUT THE GET TO MARKET TRUE QUALITY SUMMIT SERIES

September 21-24th

No matter where you're at in the process, there's a lot to plan to successfully get your device in the hands of end users and to maintain regulatory compliance across global markets.

That's why we're bringing you the Get to Market True Quality Summit Series. From napkin drawing to product launch, industry experts at this event will help guide you through processes, considerations, and regulations to make sure you're equipped with the knowledge and tips to bring your device to market (and stay there). 

Calling all a medical device company founders, key decision makers, quality managers, product development engineers, and beyond...you won't want to miss this.

Here's what you'll learn at the Get to Market Summit Series...

► What it truly means to be quality focused (and how a quality culture can impact your specific company and your medical device)

► How to tune your QMS to support your development process

► How to design labeling to optimize your regulatory strategy

► How to estimate regulatory risk and regulatory burden

► Tips for improving your pitch deck slides with key elements that help increase your chances of gaining favor with health investors

► How the design transfer records should be outlined and planned to ensure everything is documented along the way

► Market case for FDA and EU commercialization and lessons from early adopters of MDR

► How to understand medical device UDI requirements by region

► Why it’s important to do design control activities in the right order (and how to integrate risk throughout the process)

► And so much more!

PLUS, GREEN CARPET DAY

September 20th

We're rolling out the Green Carpet for this all-day virtual event dedicated exclusively to our customer community. The day is packed full of keynotes, customer-driven panels, sneak peeks of our upcoming releases and training sessions to take your Greenlight Guru usage to the next level.

**Only Greenlight Guru customers can attend this portion of the event. As a customer, you should have received an email with a special discount code.**

Building a Regulatory Strategy Executive Summary: How early in the development process should we begin to think regulatory? September 21, 2021, 06:00 PM
Mike Drues President, Vascular Sciences
Why You Need to Use IEC 62304 for Software Development September 24, 2021, 03:00 PM
Cathy Wilburn Director of Quality Assurance and Compliance, The RND Group
Understanding the Medical Device Single Audit Program (MDSAP): Pros, Cons, and How to Prepare September 23, 2021, 04:00 PM
Angelina Hakim QUNIQUE Group, Owner & CEO
Green Carpet Day (Greenlight Guru Customer Event) September 20, 2021, 04:00 PM
Greenlight Guru Team & Special Guests

This True Quality Summit Series is Highly Recommended For:

• Medical Device Executives & Leadership Teams

• Quality Professionals and Management

• Regulatory Affairs Professionals and Management

• Clinical Affairs Professionals and Management

• R&D Engineers and Management