4th Annual EU Medical Device & Diagnostic Quality Management Conference

December 4-5, 2019 | Frankfurt, Germany
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“I thought the conference was excellent!  Having a conference tailored to one discipline made each panel and contact relevant.”

Director, Compliance & Legal Affairs
Orexigen

“Great insight to hear payer perspective in contracting and account management and the changing healthcare landscape.”

Channel Liaison
Biogen

“It was definitely an excellent well-rounded opportunity to meet new people, get new ideas, and get an in-depth education on what’s to come with the FDA collaborations.”

Quality Engineer
Centurion Medical Products

“It was very well organized event and high quality, the fact to have an IVD track was also interesting. Thanks, I will recommend the Q1 event!”

Regulatory Affairs – EMEA Regional Head
BIOMERIEUX

“The organization and support staff were fantastic! I’m looking forward to next year.”

Global Business Project Lead
Genentech

About the Conference:

The guidance provided by the European Medical Device Regulation (MDR) requires a heightened level of compliance and documentation surrounding medical device product quality assurance, from increased monitoring of product surveillance to greater risk mitigation surrounding suppliers. In addition to the EU MDR, quality assurance executives are also focused on the MDSAP program, and the program’s alignment with existing quality assurance audit processes, as well as relevant ISO frameworks providing risk-mitigation guidance.

Program Highlights:

  • In-depth Discussions on MDSAP, ISO & EU MDR
  • Interactive, Industry-Driven, Collaborative Approach
  • Multiple Stakeholder Perspectives Including:
    • Industry
    • Notified Bodies
    • Regulatory Auditors
    • Legal Interpretations

Audience

75 Attendees

All attendees come directly from medical device and diagnostic companies

Distinguished Presenters

Speaker recruitment in process

Networking

Networking time is built into the agenda to allow industry peers to connect and exchange ideas

Open Dialogue and Group Share

Each presentation is followed by 10-15 minutes of open dialogue for questions and exchange of best practices

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