DT_MINN18_RandQ-logo_5-18_Vs1

DeviceTalks Minnesota is right around the corner and we couldn't possibly be more excited - really. June 4-5 is only a little over three weeks away! We've witnessed the growth of this event first-hand over the past few years and this year we're confident will be the best yet, especially considering the new partnership with the Medical Alley Association (MAA). R&Q sees this as the premier medtech event in Minnesota in 2018, which is why we've decided to be a Platinum Sponsor this year. Beyond that and most importantly, we're helping to craft the educational content of the Regulatory 2.0 track, presented by MAA. 

The Regulatory 2.0 track

Along with other accomplished industry experts with leading edge EU MDR/CER experience, we'll be contributing content to the Regulatory 2.0 track. Specifically, these sessions:

  • Transitioning from MDD to MDR: How is this REALLY rolling out? Tips, Tricks, and Lessons Learned from Large Program Implementation
  • Portfolio Planning as an Input to your EU MDR Implementation Plan. Which devices should stay and which should go? Balancing the cost and effort of transitioning to the EU MDR with product life cycle planning and revenue expectations
  • Achieving MEDDEV 2.7/1 Rev. 4 and EU MDR Compliant Clinical Evaluation Reports (CERs): What We’ve Learned From Completing 100+
  • Post-Market Surveillance Under EU MDR – Do I have to run a clinical study? What other options do you have to fulfill post market surveillance requirements; including updating CERs

There are several special presenters and panelists lined up to be formally announced soon, and they're all eager to share case studies related to the EU MDR transition. We know you're going to come away from these sessions learning something you didn't know before, and you'll likely being able to apply that information to your organization. We're sincerely looking forward to helping companies on these subjects! ...and more if you'd like to ask us. 

Stop by our booth(s)

We'll also be exhibiting at booths 204 and 206 (taking it up a notch, remember?). Stop by our booth(s) and ask us any questions related to regulatory and quality; especially the EU MDR. We'll be happy to share our knowledge, experiences, and any industry knowledge with you. Also check us out if you're interested in a career. You may think you know what consulting's all about but unless you've spoken with us, we'd ask you to reconsider those preconceived notions.

Save on registration

If you're not registered yet, you can save 20% by entering the promo code "RQ" during registration. The easiest way is to start from our exclusive sign up page...

 

Save 20% on DeviceTalks MN

 

DT_Minn_RandQ_Vs1

We are passionate about your success. Tell us more about your regulatory and quality needs so we can help.

Book a Consultation

GLOBAL BOTTOM CTA INSTRUCTIONS:

To display custom copy instead of global copy in this section, please go to Show Global Content for Bottom CTA? toggle in the "Contents" tab to the left, toggle it off, save, and then REFRESH the page editor, the custom text will then show up and ready to be edited.

Turning the global content back on will be the same process, go to the toggle and toggle it back on, save and refresh!