Are you worried that some obscure clause in the new EU MDR standard will trip your company up? Is the push to meet the deadline stressing your team out?

Attending medical device conferences that cover EU MDR can be a great way to give your team the confidence they need—and lower your anxiety level.

Don’t let the EU MDR cause you and your team sleepless nights full of worry. The more you know about the regulations, the easier it will be to follow them.

Remember, you're not alone.

Many of your peers are talking about this same subject right now. You might just have to find the right medical device conference to connect with them and join in on those conversations.

Prep for EU MDR at These 7 Medical Device Conferences

Your quality management systems are going to scrutinized closely under the EU MDR. It could be a good strategy to implement an eQMS that helps you track and record every step of your progress as you develop and manufacture your medical device.

We know that choosing the right software can be tough.

You need an eQMS that fits your unique needs and helps you maintain meticulous records, so you’re prepared for testing and audits. Qualio is an eQMS solution that was designed specifically with medical device companies in mind.

With Qualio:

  • You can create and review documents quickly with the help of our built-in templates.
  • Managers can approve and control all documents with a cloud-based system that is completely secure.
  • Your records will be safe and easily accessible, no matter where you are.

Check out our Life Sciences Quality Management Software page to learn more about Qualio and how it can help.

1. US EU MDR Implementation Conference

  • Date(s): July 2020
  • Location: Arlington, VA
  • Event Page

About the Event

The US EU MDR Implementation Conference focuses on several key topics. You’ll learn about the benefits of using a risk-based approach during the final implementation transition period and how to integrate EUDAMED into your workflows.

All of the attendees are affiliated with a medical device company, and presentations are followed by 10–15 minutes of Q&A. Networking is a huge part of the event, and they encourage peers to gather and share ideas.

Related Reading: The EU Medical Device Regulation Timeline: What You Should Know (in 2019)

2. Critical Issues for Medical Devices in 2020

  • Date(s): January 30–31, 2020
  • Location: Embassy Suites in Boston, MA
  • Event Page

About the Event

This event will focus on FDA and EU regulations for medical devices.

Attendees will learn what to expect for EU inspections and about the changes the FDA has made to some of their regulations involving cybersecurity, software, and jurisdiction.

Domestic device manufacturers, design engineers, quality assurance managers, and even business or marketing executives can all benefit from this conference.

3. MedTech Summit Dublin

  • Date(s): June 22–26, 2020
  • Location: Citywest Hotel, Dublin
  • Event Page

About the Event

Topics for this event include EU medical device regulation, post-market surveillance and vigilance, clinical evaluations and investigations, EU IVD regulation and strategy, EU medical device law, software, AI, medical device regulatory affairs in global markets, and much more.

“Deadlines for compliance with the MDR are approaching fast, and the conference provided a very direct and open update and exchange of views on the challenges and problems. It also allowed for a drill down on specific aspects of the rules, with a good practical approach.” — Peter Bogaert from Convington & Burlip LLP

Related Reading: 6 Essentials of a Clinical Evaluation Report (CER) for Medical Device Organizations

4. Medical Design & Manufacturing West Conference

  • Date(s): February 11–13, 2020
  • Location: Anaheim Convention Center in Anaheim, CA
  • Event Page

About the Event

This conference is perfect for R&D engineers, front-end product development engineers, regulatory and quality professionals, quality and process engineers, design engineers, and C-suite executives.

“It’s one-stop shopping for anybody in the product development medical device industry.”— Linda Jenkins, QA Manager from Plastics Plus Technology

Topics will include smart manufacturing, 3D printing, and risk management solutions, to name a few.

5. Drug/Device and Device/Drug Combinations in the EU and US

  • Date(s): April 2–3, 2020
  • Location: Cavendish and Rembrandt Hotels in London
  • Event Page

About the Event

This conference is for development and regulatory personnel in the pharmaceutical, diagnostic, and medical device industries.

You’ll learn everything you need to know about European regulatory guidance, how the FDA regulates combination products, and how to stay informed on post-market surveillance.

“Comprehensive overview of the drug/device and device/drug regulations in Europe and the US. Very clear and engaging presentations given by speakers with a massive experience on the field. Highly recommendable to anyone interested on this topic.” — Maria J Fernandez-Lozano, Senior Biologics Development Manager of Diamond BioPharm Limited

New call-to-action

6. FDA/Xavier MedCon Conference 2020

  • Date(s): May 5–8, 2020
  • Location: Cintas Center in Cincinnati, OH
  • Event Page

About the Event

The FDA/Xavier MedCon Conference is for medical device manufacturers and global regulators who want to learn how to protect their business, products, and patients.

“There are always a lot of FDA people onhand to be really frank and open to have[ing] conversations.” — Kim Trautman, Executive VP of Medical Device International Services, NSF International

The conference is scheduled to run for three days.

Related Reading: The Best ISO 13485 Audit Checklists on the Web

7. MedTech Conference

  • Date(s): October 5–7, 2020
  • Location: Toronto
  • Event Page

About the Event

The MedTech Conference in Toronto will feature world-class plenary speakers on a wide range of topics.

“The MedTech Conference showcases the most promising new innovations and provides content and networking that encourages interactive discussion on the state of the industry and the MedTech innovation ecosystem while facilitating valuable business opportunities.”— Ashley Wittorf, Executive Director of AdvaMed Accel and Global Head, Investor Relations of AdvaMed

EU MDR, cybersecurity, trade, inspections, M&A, AI, and precision medicine will all be discussed. More than 3,000 professionals attended the event last year in Boston.

Get Ahead of EU MDR by Improving Your Medical Device Quality

The EU MDR is going to be examining your quality management very closely. If you want to get ahead of the curve and make sure your procedures meet or exceed the guidelines, then it's time to put a focus on improving your medical device quality.

Download our free Guide to Improving Medical Device Quality. We'll show you seven things that you can implement now to help you not only boost quality but also leverage quality as a competitive advantage over the next year.

You will learn strategies to help you:

  • Improve review processes
  • Find areas where quality standards are not being met
  • How to successfully establish and utilize feedback loops
  • Ensure that your documents are in order
  • Guarantee that your team is trained appropriately

Grab your free guide and start improving your quality before EU MDR hits. New call-to-action

01-3d

We're sharing our secrets with our loyal readers. Subscribe & download it now.

01-3d

Beat the competition with better quality

Get this free guide with 7 tips to use quality to gain a competitive advantage.

Published by Robert Fenton March 10, 2020
Picture of