How to Deal with HIPAA Rules Under the Revised Common Rule
Includes a Live Event on 04/09/2019 at 2:00 PM (EDT)
(90 minutes) This webinar will provide an overview of the impact of the Common Rule (45 CFR part 46) changes on HIPAA (Health Insurance Portability and Accountability Act) (45 CFR Part 160 and Part 164) covered information and biospecimens. We will discuss the complex and varied updates and issues associated with the Revised Common Rule and how these need to be addressed when working with HIPAA covered information.
Topics to be covered will include:
- The role of HIPAA and HIPAA Controlled Data in research,
- HIPAA identifiers and biospecimen use,
- Changes to consent,
- Limited IRB review.
Melanie Clark, Associate Director, Office of Research Integrity Assurance, Georgia Institute of Technology
Carpantato (Tanta) Myles, Director, Office for Research Compliance, The University of Alabama
Handouts will be available 24 hours before the live webinar.
Closed Captioning for the live presentation is available at no additional fee. Sign in and click on the "Closed Captioning" link in the handouts tab or in the links box in the meeting room to access this feature.
Member Price: $99
Non-Member Price: $118
Your registration includes one log-in. We are pleased to provide the opportunity for you to register additional sites at a discounted price of $25.00 per log-in. When you are checking out, click the "Add" button and type in the email address of your colleague that you would like to register. If that person does not already have an NCURA profile, please have them go to the NCURA website to create a profile, then you will be able to register them with your registration. You will be able to change or add more registrations by clicking “My Registrations” in the menu at the top left of the home page, then clicking the “Purchases for Others” button. If you have any questions about this option, please email firstname.lastname@example.org.
- Participants will be able to understand the role of HIPAA and HIPAA Controlled Data in research.
- Participants will learn about HIPAA identifiers and biospecimen use in research and how these can now be used in some exempt research.
- Participants will be able to understand the changes to consent, including broad consent.
- Participants will learn about the new limited IRB review.
Carpantato (Tanta) Myles
Director, Office for Research Compliance
The University of Alabama
Associate Director, Office of Research Integrity Assurance
Georgia Institute of Technology
Participants receive 1.5 hours of continuing education credits = .2 CEU's for each webinar.
You can access your certificate from the box on the right side of the screen, after filling out the webinar evaluation.
Watching in a group? Everyone watching the presentation can request a CEU certificate by writing down the verification code at the end of the webinar. Please make a note of the verification code as it will not be available after the webinar.
The main registrant can access instructions on the Group CEU tab for group participants to receive CEU certificates.
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