7th Annual
Medical Device Regulatory Affairs Conference
June 29-30, 2022 | Chicago, IL
Overcoming Ongoing Challenges with MDR & Learning from Successful Certification Experiences while Strengthening Regulatory Compliance Strategies to Adapt to Evolving Rules in International Markets
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.
Foster a sense of collaboration and safely connect with peers and expert presenters at this intimately-sized program. Customize your experience and address your unique concerns during dynamic Q&A after each session. Our commitment to industry perspectives keeps the program focused on what matters and dynamic session types allow you to stay engaged.
Q1 PRODUCTIONS SAFEGUARD
As we welcome you back to our in-person conferences and forums, we want to assure you that providing a safe and comfortable environment in which to learn is of paramount importance to us. For the safety of all attendees, Q1 Productions will follow COVID-19 protocols to comply with CDC guidelines, state and local regulations. To learn about Q1 Productions SAFEGUARD, please click here.
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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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Reach out to us here.
“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.“
Attendees by Job Title
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Attendees by Years of Experience
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20+ Years
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15-20 Years
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10-15 Years
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Attendees by Company Size
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Less than 1k
Reach out to us with any questions.
Our team will respond promptly!
Aaron Van Dyke
Operations Director, Life Science
Q1 Productions
312-840-9086
avandyke@q1productions.com
www.q1productions.com
