REGISTRATION REQUIRED: Register here Intended Audience Faculty Research staff Fellows Students eIRB Demonstration Agenda Create protocol Application types Main eIRB panels Connected Projects sIRB functionality Comments NOTE: This session will be recorded. NOTE: This session is a duplicate of the session on Oct 1.
If you are new to the IRB or want to take a deep dive into the informed consent process, please attend our Informed Consent Process Session. IRB staff will cover definitions of informed consent, types of consent, required elements of consent, waivers of consent, and more. Target Audience: Faculty, research staff, post docs, […]
REGISTRATION REQUIRED: Register here Intended Audience Faculty Research staff Fellows Students eIRB Demonstration Agenda View IRB letters Requirements table Ancillary Review table Personnel modifications methods Amendments/CRs Request to Withdraw Submission Annual Check-Ins Task list Searching Reporting Personal profile NOTE: This session will be recorded.
REGISTRATION REQUIRED: Register here Intended Audience Faculty Research staff Fellows Students eIRB Demonstration Agenda View IRB letters Requirements table Ancillary Review table Personnel modifications methods Amendments/CRs Request to Withdraw Submission Annual Check-Ins Task list Searching Reporting Personal profile NOTE: This session will be recorded. NOTE: This session is a duplicate of the session on […]
If you are new to the IRB and in need of some guidance, please attend an IRB 101 Training Session. 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, eIRB. However, IRB […]
If you conduct clinical research with patients, and have questions about HIPAA compliance and data privacy, please attend our HIPAA Privacy Considerations for IRB Applications session. Target Audience: Penn Medicine, Penn Nursing, and Penn Dental faculty, research staff, post docs, and students. Any questions can be directed to Diana Floegel, Senior Regulatory Analyst […]
If you’re designing a study with a drug or a device – do you know if you need an Investigational New Drug (IND) or an Investigational Device Exemption (IDE) Application? Can your study be exempt from the IND or IDE regulations? Attend our Regulatory Requirements for Investigator Initiated Studies Involving Drugs and Devices training! This […]
Get ready for eIRB with eIRB 101! The IRB is excited to launch our new submission system, eIRB, in February 2026. In this session, IRB staff will review the eIRB system. Sessions will focus on how to practically use eIRB rather than how to craft materials needed for IRB review. Each eIRB 101 session will […]
Agenda Discuss updates on eIRB launch Revisit procedures for new annual check-in process Revisit new policy on automatic study closures Revisit guidance on active human research protocols migrated to the new eIRB system. Revisit required quality assurance during the first submission of a migrated study in eIRB
Get ready for eIRB with eIRB 101! The IRB is excited to launch our new submission system, eIRB, in February 2026. In this session, IRB staff will review the eIRB system. Sessions will focus on how to practically use eIRB rather than how to craft materials needed for IRB review. Each eIRB 101 session will […]