IRB 101: Biomedical Research
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 […]
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 […]
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 […]
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 […]
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 […]
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 […]
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 […]
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? […]
Penn eIRB launches on February 9 at 11am. HSERA will be view only for a year. Any research submissions must be completed through Penn eIRB. The IRB will no longer be accepting any paper or emailed submissions.
There are many support avenues as you navigate the new system, starting within the Penn eIRB submission system. Additional resources can be found on the IRB website. Click below for all information related to eIRB.