Are you new to the IRB submissions process? Attend IRB 101! IRB staff will cover types of submissions including initials, continuing reviews, modifications, and reportable events. We’ll also provide an overview of how to use the Human Subjects Research Application (HS-ERA) system to submit applications to the IRB. Any questions can be directed to Diana […]
Are you new to the IRB submissions process? Attend IRB 101! IRB staff will cover types of submissions including initials, continuing reviews, modifications, and reportable events. We’ll also provide an overview of how to use the Human Subjects Research Application (HS-ERA) system to submit applications to the IRB. Any questions can be directed to Diana […]
Are you new to the IRB submissions process? Attend IRB 101! IRB staff will cover types of submissions including initials, continuing reviews, modifications, and reportable events. We’ll also provide an overview of how to use the Human Subjects Research Application (HS-ERA) system to submit applications to the IRB. Any questions can be directed to Diana […]
Are you new to the IRB submissions process? Attend IRB 101! IRB staff will cover types of submissions including initials, continuing reviews, modifications, and reportable events. We’ll also provide an overview of how to use the Human Subjects Research Application (HS-ERA) system to submit applications to the IRB. Any questions can be directed to Diana […]
Are you new to the IRB submissions process? Attend IRB 101! IRB staff will cover types of submissions including initials, continuing reviews, modifications, and reportable events. We’ll also provide an overview of how to use the Human Subjects Research Application (HS-ERA) system to submit applications to the IRB. Any questions can be directed to Diana […]
Have questions about informed consent and the IRB review process? Join us for Informed Consent 101! We’ll cover definitions of informed consent, types of consent, required elements of consent, waivers of consent, and more. Any questions can be directed to Diana Floegel. Sign up for the session here.
The Office of the Vice Provost for Research (OVPR) is leading a critical initiative to modernize and streamline research-related information systems and business processes and provide an integrated platform that supports cutting-edge research at Penn. Research staff across the institution are encouraged to join OVPR on Monday, September 16th at 11:00 AM Eastern for updates on this program, including initiatives related to […]
If you are new to the IRB and in need of some guidance, please attend one of our IRB 101 Training Sessions. IRB staff will cover the basic types of submissions including initial applications, continuing review, modifications, deviations, and reportable events. Staff will also provide brief information about the upcoming new submission system, HRAP. However, […]
This session will provide an overview of the Response Plan for Emergencies Impacting Penn’s Human Research Protections Program (Penn IRB SOP GA 108) to ensure the rights and welfare of research participants during an emergency. This session will also review the Emergency Risk Mitigation Planning Guidance providing investigators with guidance for developing protocol-specific plans to […]
If you are new to the IRB or want to take a deep dive into the informed consent process, please attend our Informed Consent 101 Training Session. IRB staff will cover definitions of informed consent, types of consent, required elements of consent, waivers of consent, and more. This session will be relevant to all schools […]