5th Annual
EU IVD Clinical & Regulatory Conference
Date TBD | Location TBD
Master European IVD regulation requirements to execute compliant strategies for clinical trials & successful submissions
Program Overview
Lead organizational change to ensure clinical and regulatory processes are compliant with EU IVDR. Global regulatory stakeholders clarify guidance and best practices to demonstrate real-life product efficiency, including executing clinical trials that garner sufficient evidence. Exchange lessons learned in application submission processes and benchmark appropriate budget and resource allocation with peers.
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.
“Many thanks for all your efforts on running this program…a well-deserved toast! Certainly do share our grateful sentiment to your other ‘Dream Team’ colleagues as well.”
Jennifer Dacpano-Komansky, Director Global Regulatory Affairs, Medical Devices, Novartis
The Q1 Productions Event Experience
Are You a Solution Provider?
Reach out to us here.
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
