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 […]
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? […]