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FDAnews/CenterWatch Announces -- Informed Consent: Human Subject Protection in the Digital Health Age Webinar, Mar. 31, 2020
  • USA - English

Protect human subjects in the digital age. Learn the latest on informed consent for data acquired from apps, wearables and more.


News provided by

CenterWatch

Mar 17, 2020, 00:00 ET

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WCG CenterWatch
WCG CenterWatch

FALLS CHURCH, Va., March 17, 2020 /PRNewswire-PRWeb/ -- Informed Consent
Human Subject Protection in the Digital Health Age
An FDAnews/CenterWatch Webinar
Tuesday, March 31, 2020, 1:30-3:00 p.m. EDT
https://www.centerwatch.com/informedconsent

In today's digital age, it's not uncommon for people to regularly share their personal healthcare data with everything from medical apps to wearables to clinical decision software.

Knowing whether this information is subject to informed consent and how it can be used for research purposes is critical for any clinical trials executive.

Does one have a good grasp on the latest regulations of digital technologies and how it will affect trials and product development?

Join CenterWatch and experts Michael Werner and Sara Klock for a comprehensive webinar on how to comply with FDA and other federal regulation of digital technologies March 31:

● Assess how digital technologies used to gather, analyze and report healthcare data for medical treatment purposes or to promote a healthy lifestyle can also be used for research purposes
● Familiarize oneself with the regulatory landscape to understand how digital technologies and the information they gather and use in research will be regulated
● Determine how to design clinical trials using digital technologies that comply with the 21st Century Cures Act and changes to the Common Rule
● Identify what activities can be undertaken to develop new digital technologies without triggering federal research regulations
● Find out how to develop informed consent forms when Institutional Review Board oversight is required, and other compliance questions
● Identify factors likely to determine whether and to what extent certain technologies are regulated as medical devices by FDA

In the era of digital information collection, ones needs to know how to gather, analyze and report healthcare data that is obtained electronically.

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:
Informed Consent
Human Subject Protection in the Digital Health Age
An FDAnews/CenterWatch Webinar
Tuesday, March 31, 2020, 1:30-3:00 p.m. EDT
https://www.centerwatch.com/informedconsent

Tuition:
$287 per site

Easy Ways to Register:
Online: https://www.centerwatch.com/informedconsent
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 CenterWatch

Related Links

https://www.centerwatch.com/

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