FDAnews Announces -- Get Pre-Certified: Software as a Medical Device Webinar, August 1, 2019

FALLS CHURCH, Va., July 23, 2019 /PRNewswire-PRWeb/ -- Is there some way to bring a software as a medical device (SaMD) product to market faster? The answer is yes, with the Software Precertification Program.

The pre-cert pathway regulatory model expedites pre-market approval while assessing the safety and effectiveness of software technologies.
Attend this webinar to increase ones chances of pre-certification:

• Understand how to streamline the premarket review
• Leverage information and data obtained during pre-cert
• Learn how to establish a more modern and tailored approach toward software integration

Companies who participated in the FDA's pilot phase include major manufacturers, such as Apple, Fitbit, Johnson & Johnson, Roche, Samsung, and Verily.

Interested in registering multiple sites?
Call (888) 838-5578 in the U.S. or +1 (703) 538-7600 globally
to learn about our special multisite discount.

Webinar Details:
Get Pre-Certified: Your Software as a Medical Device
**An FDAnews Webinar**
Thursday, Aug. 1, 2019 · 1:30 p.m. - 3:00 p.m. EDT
https://www.fdanews.com/getprecertified

Tuition:
$287 per site

Easy Ways to Register:
Online: https://www.fdanews.com/getprecertified
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