Showing results for IRB

How to Conduct an Audit of a Ceded Study
Presented by: Leslie Howes, MPH, CIP - Harvard T.H. Chan School of Public Health Learning Objectives: Identify ways to assess your cede...
Consent with Subjects Who Do Not Speak English
Focuses on the role that language plays in developing consent processes and obtaining consent in study populations that do not speak English. It ident...
Understanding Consent Requirements and “Key Information” Under the Revised Rule
Presented by: Misti Ault Anderson, MS, MA – HHS Office for Human Research Protections This webinar provides learners with a review of the new reg...
Biomed Refresher 1 – Regulations and Process
Defines “research” and “human subject,” identifies different types of exempt research, and discusses the process for expedited review. Also di...
Biomed Refresher 1 – Informed Consent
Reviews key concepts from the basic module Informed Consent. Identifies the process of informed consent, describes the steps necessary to ensure human...
Update to OHRP's Incident Reporting System
As of January 2, 2022, institutions will be required to submit OHRP incident reports, electronically, via the new online form (unless they are unable ...
Detecting and Evaluating Adverse Events
Defines adverse events (AEs) and related clinical trial terminology in accordance with ICH guidelines. Describes the process for identifying AEs in cl...
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