eIRB Townhall: Protocol Migration Guide
ZoomAgenda Provide guidance on active human research protocols migrated to the new eIRB system. Outline required quality assurance during the first submission of a migrated study in eIRB
Agenda Provide guidance on active human research protocols migrated to the new eIRB system. Outline required quality assurance during the first submission of a migrated study in eIRB
Agenda Procedures for new annual check-in process Automatic study closures
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.
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 […]
Are you an ethnographer who’s wondering how to submit your project to the IRB? Please attend our Ethnographic Submissions Training! IRB staff will explain how to translate your work into an IRB application and cover what the IRB looks for when reviewing ethnographic projects. Target Audience: Social science and Humanities faculty, research staff, post […]