eIRB Townhall: Review of Policy Changes
ZoomAgenda Procedures for new annual check-in process Automatic study closures
10 events found.
Biomedical Research
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IRB 101: Biomedical Research
ZoomIf 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 […]
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eIRB Demo: Research Staff, Part 1
ZoomREGISTRATION 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.
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eIRB Demo: Research Staff, Part 1
ZoomREGISTRATION 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.
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IRB 101: Informed Consent Process
ZoomIf 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, […]
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eIRB Demo: Research Staff, Part 2
ZoomREGISTRATION 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.
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eIRB Demo: Research Staff, Part 2
ZoomREGISTRATION 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 […]
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IRB 101: Biomedical Research
ZoomIf 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 […]
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IRB 101: HIPAA Privacy Implications for IRB Applications
ZoomIf 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 […]
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IRB 101: Regulatory Requirements for Investigator Initiated Studies Involving Drugs and Devices
ZoomIf 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 […]