image goes here
Is Your Site Ready to Conduct Gene Therapy Research?
The world has officially been introduced to mRNA, and we were surprisingly comfortable with the idea of taking genetically engineered treatments. Gene therapy-based products are entering human trials at an exponential growth rate. Is your site ready to participate?
In this webinar we will take a look at the basics of conducting human gene therapy research, requirements for institutional biosafety committee (IBC) review as outlined in NIH Office of Science Policy guidelines, and prepare you and your site to be ready when the next human gene therapy trial comes along.
- Define the basic regulations and guidelines governing IBCs and gene therapy research
- Outline key takeaways to prepare your research site to participate in this growing field of research
- Explain the role of the IBC and how their oversight is different than IRB
MCSE, CIP, CPIA, CRQM
Vice President, Research Services & Strategic Consulting
Who should watch?
This content applies to research professionals representing sponsors, CROs, institutions, and sites who are involved in research pertaining to infectious disease vaccines, oncology, immune therapy and gene therapy.
This session meets the Certified IRB Professional (CIP) recertification guidelines for a maximum of 1 credit.
The Society of Clinical Research Associates (SOCRA - www.SOCRA.org) accepts documentation of candidate participation in continuing education programs for recertification if the program is applicable to clinical research regulations, operations or management, or to the candidate’s clinical research therapeutic area. This program offers 1 hour of CE credit.
If you would like to obtain CE credits for a different credential, please check with your professional organization to determine if our webinars meet their continuing education requirements.
Certificate of Attendance
After watching this webinar in its entirety and completing the webinar survey, you will receive a certificate of attendance. This certificate will be emailed to you within one business day of watching the webinar. Please note that if your organization has other staff members who wish to get a certificate of attendance, each person must register, watch the webinar in its entirety, and complete the webinar survey. Visit our Webinar Help page for more information on certificates of attendance.
DATE: June 23, 2021
Time: 3 pm ET | 12 pm PT
Duration: 1 hour