Office of Research Upcoming Training Events - Office of Research

Upcoming Training Events

Trust, Technology and Consent in the Era of New Common Rule

OHRP Research Community Forum

Date: TBD
Location: Silver Legacy Resort & Casino | Reno, NV


 

CTSC: Clinical Research Drop-in Office Hours

1st Fridays – Health Data – Health Library Informatics
2nd Fridays – Regulatory Overview & IRB Requirements
3rd Fridays – EMR Research Application
4th Fridays – REDCap Database Building & Management

Time: 12:00-2:00 pm

Where: Zoom
Registration: Not required

Additional Information: https://health.ucdavis.edu/ctsc/eventcalendar/index.html


 

CTSC: Single IRB and RELIANCE REG 160 

Date: TBD

Time: 9am-10am

Location: Zoom

Cost: No cost

Registration: Register at LMS

Join representatives from IRB Administration to learn about the new Single IRB requirements for multi-site research mandated by the 2018 Common Rule. During this interactive course, we will also discuss NIH-funded Single IRB requirements, when a reliance is appropriate in multi-site research and how to submit a complete IRBNet application to UCD IRB when a reliance is requested.

Zoom advance registration is required. Zoom registration information will be sent after LMS registration is completed.


 

CTSC: Outside Financial Conflicts of Interest in Research REG 120

Date: February 16, 2021

Time: 9am-10am

Location: Zoom

Cost: No cost

Registration: Register at LMS

Zoom advance registration is required. Zoom registration information will be sent after LMS registration is completed.


 

CTSC: ICF Fundamentals – Pt. 1: Developing Informed Consent Documents REG 130

Date: March 4, 2021

Time: 9am-10am

Location: Zoom

Cost: No cost

Registration: Register at LMS

In Part 1 of this interactive course, we will focus on developing the consent document. Representatives from IRB Administration will discuss the legal requirements of consent documents, highlight common problems, and provide practical tips to improve your application to the IRB. Attendees will review a consent document from the IRB’s perspective to determine if it meets the criteria for approval. We will also discuss options for developing consent documents when language barriers exist.

Zoom advance registration is required. Zoom registration information will be sent after LMS registration is completed.


 

CTSC: IRB – New Projects Submissions REG 170

Date: March 23, 2021

Time: 9am-10:30am

Location: Zoom

Cost: No cost

Registration: Register at LMS

Designed for researchers new to human subjects research at UC Davis and who submit new project submissions to the IRB. Attendees will learn when and how to apply for IRB review, what the IRB is looking for during the review process, and how to navigate our electronic submission system, IRBNet. During this interactive course we will focus on the process of submitting a new projects application and corresponding with the IRB. Attendees should create an IRBNet account prior to attending class.

Zoom advance registration is required. Zoom registration link will be sent after LMS registration is completed.


 

CTSC: IRB Reporting Requirements: Minor Deviations and Reportable Events REG 230

Date: April 22, 2021

Time: 9am-10am

Location: Zoom

Cost: No cost

Registration: Register at LMS

Designed for researchers new to human subjects research at UC Davis and who submit new project submissions to the IRB. Attendees will learn when and how to apply for IRB review, what the IRB is looking for during the review process, and how to navigate our electronic submission system, IRBNet. During this interactive course we will focus on the process of submitting a new projects application and corresponding with the IRB. Attendees should create an IRBNet account prior to attending class.

Zoom advance registration is required. Zoom registration link will be sent after LMS registration is completed.


 

CTSC: IRB – Post Approval Submissions REG 180

Date: April 27, 2021

Time: 9am-10am

Location: Zoom

Cost: No cost

Registration: Register at LMS

Designed for researchers new to human subjects research at UC Davis and who submit post approval submissions to the IRB. Attendees will learn when and how to maintain IRB approval, what the IRB is looking for during the review process, and how to navigate our electronic submission system, IRBNet. During this interactive course we will focus on the process of post approval submissions, corresponding with the IRB, and securing approval documents to maintain compliance. Attendees should create an IRBNet account prior to attending class.

Zoom advance registration is required. Zoom registration link will be sent after LMS registration is completed.

The IRB has redesigned its section on this site. Please update page bookmarks and links as needed.