FDAnews Announces --17th Annual Medical Device Quality Congress April 20-22, 2020 - Bethesda, MD

Manage EU quality programs before the May 26 deadline -- hear from FDA officials, industry experts at Medical Device Quality Congress.

News provided by

FDAnews

Jan 22, 2020, 00:00 ET

FALLS CHURCH, Va., Jan. 22, 2020 /PRNewswire-PRWeb/ -- 17th Annual Medical Device Quality Congress
Monday, April 20 – Wednesday, April 22, 2020
The Bethesdan Hotel • Bethesda, MD
https://www.fdanews.com/mdqc?hittrk= 20122VOCUS [https://www.fdanews.com/mdqc __title__ MDQC]

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

A special focus on the new EU Medical Device Regulation (EU-MDR) will ensure compliance in Europe. With the Medical Device Quality Congress taking place weeks before the May 2020 EU-MDR deadline, attendees will easily fine-tune plans — and strengthen product positions — in advance of these sweeping changes.

The Medical Device Quality Congress's sessions will cover US and international critical 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 must know to obtain a CE Mark
  • QMS under EU-MDR and EU-IVDR — create a foolproof QMS
  • Complaint reporting — save time and money by avoiding resubmission requests with US medical device reporting (MDR) and EU-MDR's/IVDR's new manufacturer's incident report (MIR)
  • Corrective actions — US 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 the calendar for April 20-22 to interact with FDA officials, consultants, lawyers, experts and colleagues — before EU-MDR's deadline. Make reservations early: The Bethesdan Hotel is the perfect setting for the Congress and its ample networking events. It's also equally convenient to both FDA headquarters and Washington, D.C.

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

Early Bird up to $400 discount!
Sign up through March 23 and get up to $400 off the regular price.

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

Conference Details:
17th Annual Medical Device Quality Congress
Monday, April 20 – Wednesday, April 22, 2020
The Bethesdan Hotel • Bethesda, MD
https://www.fdanews.com/mdqc?hittrk= 20122VOCUS [https://www.fdanews.com/mdqc __title__ MDQC]

Tuition:
Early Bird Pricing: $1,597 (available until Mar. 23, 2020)
Regular Pricing: $1,797 (after Mar. 23, 2020)
Significant team discounts are available.

Easy Ways to Register:
Online: https://www.fdanews.com/mdqc?hittrk= 20122VOCUS [https://www.fdanews.com/mdqc __title__ 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.

SOURCE FDAnews