- Events
- IRB/HSPO
IRB/HSPO
IRB Board C Review Meeting
WebconferenceIRB Board C will meet to review protocols.
Webinar: Research Document Management
WebconferenceIn this workshop offered by Penn State's Institutional Review Board (IRB), participants will review the good clinical practice (GCP) definitions and regulations for research data management and define source documentation and list examples.
IRB Board A Review Meeting
WebconferenceIRB Board A will meet to review protocols.
Webinar: IRB Informed Consent training
WebconferenceThis IRB/HSPO training session for those involved with human subjects research at Penn State will focus on several topics in research consent.
Webinar: IRB Overview Training
WebconferenceThis training provides an overview of human subjects research at Penn State and will be presented by Courtney Karmelita.
Webinar: IRB Board B Review Meeting
WebconferenceIRB Board B will meet to review protocols.
IRB Board C Review Meeting
WebconferenceIRB Board C will meet to review protocols.
IRB Board A Review Meeting
WebconferenceIRB Board A will meet to review protocols.
Webinar: IRB Board B Review Meeting
WebconferenceIRB Board B will meet to review protocols.
IRB Board C Review Meeting
WebconferenceIRB Board C will meet to review protocols.
IRB Board A Review Meeting
WebconferenceIRB Board A will meet to review protocols.
Webinar: Reportable New Information (RNI) Workshop
WebconferenceIn this workshop offered by Penn State's Institutional Review Board (IRB), participants will review the basis for requiring reporting of new information in research, define what constitutes reportable new information and discuss reporting time requirements.
Webinar: IRB Informed Consent training
WebconferenceThis IRB/HSPO training session for those involved with human subjects research at Penn State will focus on several topics in research consent.
IRB Board C Review Meeting
WebconferenceIRB Board C will meet to review protocols.
Webinar: Research Document Management
WebconferenceIn this workshop offered by Penn State's Institutional Review Board (IRB), participants will review the good clinical practice (GCP) definitions and regulations for research data management and define source documentation and list examples.