Mar 7, 2019   SOURCE: PR NewsWire

FDAnews Announces -- Medical Imaging: Latest Regulatory, Compliance and Quality DevelopmentsWebinar, March 19, 2019

FALLS CHURCH, Va., March 7, 2019 /PRNewswire-PRWeb/ -- Medical Imaging
Latest Regulatory, Compliance and Quality Developments
**An FDAnews Webinar**
Tuesday, March 19, 2019, 1:30 p.m. - 3:00 p.m. EDT
http://www.fdanews.com/medicalimaging

Ultrasound imaging... MRI... pediatric x-ray imaging... medical x-ray imaging... radiography... computed tomography... fluoroscopy... mammography...

As electronic technology advances, its integration into medical devices -- specifically medical imaging devices -- challenges the FDA to regulate the integrated devices and still allow new technologies to the market in a reasonable time.

J. Lawrence Stevens, RAC -- an expert witness for cases involving FDA compliance for medical devices -- will discuss the latest FDA trends and how to keep companies competitive. After attending this webinar, attendees will understand: 

    --  The nuances of the latest in FDA premarket and post market requirements
        for medical imaging devices
    --  How to comply with Title 21 - Food and Drugs, Chapter 9, FA&C Act,
        Subchapter V, Drugs and Devices
    --  How to comply and interpret FDA's Guidance on Display Devices for
        Diagnostic Radiology - Guidance for Industry and Food and Drug
        Administration Staff Issued Date 10/02/17
    --  What the recent article, "The Long Run Is Now: How FDA is Advancing
        Digital Tools for Medical Product Development," by Lauren Silvis, FDA
        Chief of Staff means for medical imaging regulation

This is a chance to hear from an expert on FDA medical device regulation on how the FDA is using its authority in the new generation of medical imaging devices.

Meet Your Presenter:
J. Lawrence Stevens, RAC
Mr. Stevens has over 20 years of FDA experience encompassing virtually all of the FDA field positions. He also has eighteen years of industry experience as a mid-level manager and senior executive in clinical, regulatory, and quality in the medical device industry. He currently serves as an expert witness for cases involving FDA regulation compliance for medical devices. He regularly performs webinars regarding FDA and issues regarding clinical studies and medical devices.

Who Will Benefit: 

    --  CEO's
    --  VP RA/QA
    --  VP R&D
    --  Directors of RA
    --  Directors of R&D

Webinar Details:
Medical Imaging
Latest Regulatory, Compliance and Quality Developments
**An FDAnews Webinar**
Tuesday, March 19, 2019, 1:30 p.m. - 3:00 p.m. EDT
http://www.fdanews.com/medicalimaging

Tuition:
$287 per site

Easy Ways to Register:
Online: http://www.fdanews.com/medicalimaging
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