2021 State of Medical Device Virtual Summit by Greenlight Guru

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WHAT TO EXPECT AT THE 2021 STATE OF MEDICAL DEVICE VIRTUAL SUMMIT

How will COVID-19, new programs and regulatory changes on the horizon, as well as technological shifts and trends impact your medical device company in 2021?

With uncertainty still looming, what will it take to plan for the future, while staying flexible enough to quickly pivot when challenges are thrown your way?

The 2021 State of Medical Device Virtual Summit is for quality, regulatory, and product development professionals to understand the strategies, tactics and technologies being used today and uncover best practices, tips, and trends for the evolving nature of the industry.

The two day, digital event dives into perspectives, predictions, and experiences of industry leaders and takes a deep dive into the insightful findings from Greenlight Guru’s State of Medical Device Product Development and Quality Management Report.

Now's your chance to uncover what it takes for your company to move forward and succeed in 2021.

Strategies for Improving Medical Device Software and Cybersecurity 09 December 2020, 04:00 PM

Chris DuPont, Christopher Gates, Pooja Kartik, Shane Keating & Cathy Wilburn

Software as a Medical Device (SaMD) Challenges and Opportunities for 2021 and Beyond 09 December 2020, 03:00 PM

Tom Rish & Andrew Wu Greenlight Guru & Rook Quality Systems

A Delay in MDR: Where are We Now? 09 December 2020, 06:15 PM

Thor Rollins & Karen Schuyler Nelson Laboratories, LLC & Subject Matter Expert

Implementing a Global Unique Device Identification (UDI) Solution: Regional Update and Requirements 09 December 2020, 02:00 PM

John Lorenc, Barret Mueller & Gary Saner

This Virtual Summit 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

The 2021 State of Medical Device Virtual Summit is for you if you are:

• Looking to get ahead of the regulatory changes and trends coming in 2021

• Ready to understand strategies, tactics, and technologies today’s medical device professionals are using to accelerate product development, ensure compliance, and promote quality

• Forward-thinking, and recognize the importance of planning for the future, while staying flexible enough to pivot quickly

• Wanting to learn what market-leading companies are doing to prepare for the future (and how your organization can do the same)

• Facing uncertainty with the COVID-19 pandemic and looking for resources to provide clarity

• Advocate for shifting compliance-minded organizations to a True Quality focus