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7th Annual

Medical Device Regulatory Affairs Conference

June 29-30, 2022 | Virtual Event

Overcoming Ongoing Challenges with MDR & Learning from Successful Certification Experiences while Strengthening Regulatory Compliance Strategies to Adapt to Evolving Rules in International Markets
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Program Overview

This event brings together regulatory, legal, and global regulatory agency perspectives to share strategies and methodologies on current challenges faced by medical device regulatory affairs teams working to secure product approval. Explore how your peers educate and engage internal stakeholders in clinical research/performance evaluation, quality assurance and post-market surveillance to gather and fulfill submission requirements in multiple global markets. Case studies and group discussions highlight practical experiences among shifting regulatory expectations.

The dynamic Q1 Productions virtual platform fosters a sense of collaboration. Thoughtfully designed networking features connect you with your peers beyond the capabilities of a Zoom meeting. Customize your experience and address your unique concerns during live Q&A after each session. Our commitment to industry perspectives keeps the program focused on what matters and dynamic session formats to increase interactivity and strategy-building.

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Experience the Quality First Difference.

Learn from Industry Leaders

An exclusive experience with professional thought leaders provides you with direct insight into current solutions.

Keep up with Industry Trends

Learn through dynamic panel discussions, case studies and real world evidence on current topics directly related to your industry.

Exchange Ideas & Network

We provide a platform for your team to ask questions with experienced industry experts. The key to building your knowledge and seeing things from another perspective.

Find Solutions that Work for You

Insight and interaction are at the ready for you and your team. Collaborate with your peers, utilizing their insight and experience to accommodate your common challenges.

“I gained information on the path industry is taking. The Q1 staff were all a joy to work with.”

Mitch Mallough, Program Engineer III, Johnson & Johnson

Distinguished Presenters Include:

Balazs Bozsik
Technical Director – Medical Audit
SGS North America, INC.

William Brodbeck
Sr. Director, Regulatory Affairs
Steris

Roger Peterson, MSc
Sr. Mgr, Global Labeling – Regulatory Operations
Arthrex

The Q1 Productions Event Experience

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Our Sponsors

Media Partner:

I really believe this conference was top-notch. I must say you do a fantastic job in coordinating and producing these events, and I’ve been a part of many. I thought the conference exceeded expectations.

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Reach out to us with any questions.

Our team will respond promptly!

Chris Cockerell
Chris Cockerell
Senior Event Manager
Q1 Productions
+1 (312) 224-8722
ccockerell@q1productions.com

www.q1productions.com