5th Annual EU Medical Device and Diagnostic Quality Management Conference

December, 2020 | Frankfurt, Germany

5th Annual EU Medical Device and Diagnostic Quality Management Conference
December, 2020 | Frankfurt, Germany

Request Invite

WE GUARANTEE 100% PRIVACY, YOUR INFORMATION WILL NOT BE SHARED

“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:

With the impact of the new regulatory framework in Europe and tight timeframes for compliance, device and diagnostic quality executives continue to focus efforts on updating QMS processes to reflect new and enhanced provisions, all while ensuring ongoing operations are not disrupted. One of the most prominent challenges lies in the reorganization of end-to-end supply chain operations with the new definition of Economic Operators and incumbent responsibilities for which supplier partners, distributors and importers in particular must be efficiently and swiftly trained. In addition, supplier control is at the forefront of both industries’ concern to ensure visibility into partners’ quality systems and ultimately guarantee end-product compliance, as well as long-lasting business relationships.

Core Topics to Be Addressed:

  • MDR auditors’ focus, new areas of challenge and lessons learned
  • Strategies to enhanced supplier quality control while containing costs
  • Integrating new economic operator considerations into supply chains
  • PMS & PMCF Guidance: Promoting collaboration for clinical & quality teams
  • EUDAMED: Technical considerations for compliance readiness deadline

Program Highlights:

  • Addressing perspectives from Notified Bodies and auditors
  • Strategy & solution exchanges through interactive session formats
  • Best practices from peers’ experience in overcoming timely challenges

Core Topics to Be Addressed:

  • MDR auditors’ focus, new areas of challenge and lessons learned
  • Strategies to enhanced supplier quality control while containing costs
  • Integrating new economic operator considerations into supply chains
  • PMS & PMCF Guidance: Promoting collaboration for clinical & quality teams
  • EUDAMED: Technical considerations for compliance readiness deadline

Request Invite

WE GUARANTEE 100% PRIVACY, YOUR INFORMATION WILL NOT BE SHARED

Audience

75 Attendees

All attendees come directly from medical device and diagnostic companies

Distinguished Presenters

Speaker recruitment in progress

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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