FDAnews Announces 17th Annual Medical Device Quality vCongress Oct. 7-8, 2020

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Manage EU quality programs before the May deadline — hear from FDA officials and industry experts at Medical Device Quality vCongress.

WCG CenterWatch

WCG CenterWatch

17th Annual Medical Device Quality vCongress
Thursday, Oct. 8, 2020 • 1:00 p.m.-4:15 p.m. EDT
https://www.fdanews.com/mdqc

Attend the premier event for device quality and compliance professionals: the 17th Annual Medical Device Quality vCongress. This virtual program is filled with up-to-the-minute topics needed to manage quality programs in the U.S. and EU.

A special focus on the new EU Medical Device Regulation (EU-MDR) will ensure one’s compliance in Europe. With the Medical Device Quality vCongress taking place a few months before the May 2021 EU-MDR deadline, attendees can easily fine-tune plans — and strengthen product positions — in advance of these sweeping changes.

The Medical Device Quality vCongress’s virtual sessions will cover critical U.S. and international topics, including:

  • Impact of new economic operators in the EU-MDR and EU In Vitro Diagnostics Regulation (EU-IVDR) — the key to business success in the EU
  • Implementation of the clinical evaluation (EU-MDR) or performance evaluation process (EU-IVDR) — what one needs to know to obtain a CE Mark
  • Quality management system (QMS) under EU-MDR and EU-IVDR — create a foolproof QMS
  • Complaint reporting — save time and money by avoiding resubmission requests with U.S. medical device reporting (MDR) and EU-MDR’s/IVDR’s new manufacturer’s incident report (MIR)
  • Corrective actions — U.S. and EU perspectives, including EU-MDR/IVDR field safety corrective actions (FSCAs), field safety notice (FSN) and other reports one must file to ensure compliance
  • Risk management systems (RMS) under ISO 14971:2019, including European norms — practical ways to implement both in one unified system
  • Postmarket surveillance (PMS) in EU-MDR/IVDR — take a more proactive approach and implement a compliant system

Mark your calendar for Oct. 7-8 to interact virtually with FDA officials, consultants, lawyers, experts and colleagues — before EU-MDR’s deadline. This virtual event provides all the benefits of a live MDQC but allows you to attend remotely. No travel, no hassle!

This is 2020’s most important event for devicemakers: the 17th Annual Medical Device Quality vCongress.

Multi-attendee discounts available!
Significant tuition discounts are available for teams of two or more from the same company.

Virtual Conference Details:
17th Annual Medical Device Quality vCongress
Thursday, Oct. 8, 2020 • 1:00 p.m.-4:15 p.m. EDT
https://www.fdanews.com/mdqc

Tuition:
Regular Pricing: $697

Easy Ways to Register:
Online: https://www.fdanews.com/mdqc
By phone: 888.838.5578 or 703.538.7600

About FDAnews:
FDAnews is the premier provider of domestic and international regulatory, legislative, and business news and information for executives in industries regulated by the US FDA and the European Medicines Agency. Pharmaceutical and medical device professionals rely on FDAnews' print and electronic newsletters, books and conferences to stay in compliance with international standards and the FDA's complex and ever-changing regulations

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Michelle Butler
FDAnews
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