Session Description |
Session Recording |
What Needs Review (Medical Research)
We’ve been making more use of flexibility in the regulations and adopting more industry best practices to better tailor our reviews to risk.
This webinar covers:
- How we’re re-calibrating the jurisdiction of Human Research Protections Program (HRPP) and the IRB
- How you can anticipate what type of review you’ll need for different types of projects (or that you won’t need a review)
- What’s involved in the different types of review, including certain clinical activities that require IRB review such as humanitarian use devices or expanded access to investigational drugs for treatment
- How Kuali IRB is designed to lead you through, based on your project's requirements
|
Watch Session Recording
AD login required
|
Informed Consent (Medical Research)
We rolled out a new informed consent template!
This webinar discusses:
- Key changes to the form
- Updates in areas like surrogate consent and short-form consent
- Basics and urban legends around
- Consent-related waivers
- HIPAA & research
- Consent process and documentation
|
Watch Session Recording
AD login required
|
What Needs Review (Social/Behavioral/Educational Research)
We’ve been making more use of flexibility in the regulations and adopting more industry best practices to better tailor our reviews to risk.
This webinar covers:
- How we’re re-calibrating the jurisdiction of Human Research Protections Program (HRPP) and the IRB
- How you can anticipate what type of review you’ll need for different types of projects (or that you won’t need a review)
- What’s involved in the different types of review
- How Kuali IRB is designed to lead you through, based on your project's requirements
|
Watch Session Recording
AD login required
|
Informed Consent (Social/Behavioral/Educational Research)
We rolled out a new informed consent template!
This webinar will discuss:
- Key changes to the form
- Basics and urban legends around:
- Consent-related waivers
- FERPA & research
- Consent process and documentation
|
Watch Session Recording
AD login required
|
Your Existing Research Before and After Kuali Go-Live (Medical Research)
Although new research has gotten a fresh start in Kuali IRB, there will be a yearlong rolling transition for projects that are already active in our legacy system.
This webinar covers:
- How the transition will impact different types of projects
- How to plan ahead to make the transition as smooth as possible for everyone
|
Watch Session Recording
AD login required
|
Your Existing Research Before and After Kuali Go-Live (Social/Behavioral/Educational Research)
Although new research has gotten a fresh start in Kuali IRB, there will be a yearlong rolling transition for projects that are already active in our legacy system.
This webinar covers:
- How the transition will impact different types of projects
- How to plan ahead to make the transition as smooth as possible for everyone
|
Watch Session Recording
AD login required
|
Multisite Research and the Single IRB (All Audiences)
More and more multisite research is undergoing review by only one IRB instead of multiple IRBs.
Maybe you’re partnering with local schools or healthcare organizations.
These arrangements aren’t necessarily easier (yet) and often require diligent communication.
This webinar covers:
- How we’re simplifying our part in the process through:
- Simpler documentation requirements
- Expanded use of commercial IRBs
- How Kuali IRB will help
|
Watch Session Recording
AD login required
|
Post-Approval Responsibilities (Medical Research)
This is a refresher on ongoing responsibilities as you conduct research.
This webinar covers:
- What changes to submit and when
- What problems to report and when
- Continuing reviews (if still required) and closures
- Preview of how Kuali IRB changes and simplifies these ongoing interactions with the Human Research Protections Program (HRPP) and the IRBs
|
Watch Session Recording
AD login required
|
Post-Approval Responsibilities (Social/Behavioral/Educational Research)
This is a refresher on ongoing responsibilities as you conduct research.
This webinar covers:
-
- What changes to submit and when
- What problems to report and when
- Continuing reviews (if still required) and closures
- Preview of how Kuali IRB changes and simplifies these ongoing interactions with the Office of IRB Administration (OIA) and the IRBs
|
Watch Session Recording
AD login required
|