Showing results for IRB

Biomed Refresher 1 – Records-Based Research
Identifies what levels of regulatory authority apply to research with records, describes the steps to ensure the protection of privacy and confidentia...
Informed Consent - SBE
Discusses the process and documentation of informed consent, including informed consent guidelines as well as the required and additional elements of ...
Navigating the Transition from ICH E6(R2) to ICH E6(R3): Key Changes and Best Practices for Clinical Trial Sites
The International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH) E6 guideline for Good Clinical Practice ...
Illegal Activities or Undocumented Status in Human Research
Provides training and insight to researchers, administrators, and institutional review boards (IRBs) regarding added risks and challenges of conductin...
Institutional Oversight of Human Research
This module explains the requirements for research institutions and IRBs for ensuring regulatory compliance and oversight of research to protect human...
Research Involving Subjects at the End-of-Life
Persons at the end of life may be vulnerable for numerous reasons, including cognitive and physical impairments, which may progress as death approache...
On Tech Ethics Podcast - Use of RealResponse in Fostering Safe and Inclusive Work Environments
Season 1 - Episode 18 - Use of RealResponse in Fostering Safe and Inclusive Work Environments Discusses RealResponse, which is a platform that helps ...
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