Showing results for IRB

Biomed Refresher 3 – Regulations and Process – IRB Authority and Composition
Summarizes what the IRBs are authorized to do by federal regulations and describes the required composition of an IRB. Based on module Basic Instituti...
Biomed Refresher 3 – Regulations and Process – IRB Responsibilities
Considers key concepts of regulatory responsibilities of the IRB related to the requirements for approval of research involving human subjects from th...
IRB Review of Informed Consent
This module provides a deeper dive into the review of informed consent. We touch on regulatory requirements and critical areas of IRB review of inform...
Implementing SOPs and Working with the IRB
Discusses the rationale and importance of creating and using SOPs in research. Describes the requirements for IRB review, defines the process for obta...
FDA Issues New COVID-19 Guidance for IRBs and Clinical Investigators
In order to support response efforts to this pandemic, the FDA has issued guidance to provide non-binding recommendations regarding the key factors an...
1 … 11 12 13 14 15 … 85

Can't Find What You're Looking For?

Search Support Center for additional results

Search Support Center