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 […]
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? […]