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, […]
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, IRB 101 will […]
If you’re designing a study with a drug or device (e.g., lab test, software application, or other device product) – 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 […]
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 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, […]
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 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 […]
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 […]