During this webinar, the speaker will cover the role of the IRB; IRB application and user registration processes; required human subject protection training; research project submissions; and post-approval functions in clinical research.
This web session will help learners understand research misconduct, the guidelines pertaining to research misconduct, and the best ways to promote responsible research practices.
In this module, participants will have a better understanding of the impact of health literacy on informed consent and review a typical research consent document.
In this webinar, the speaker will discuss patient health literacy, why health literacy is important to public health, and why healthy literacy is important in clinical trials and pediatric trials.
This module identifies pediatric assent regulations, how the regulations relate to ethics, and provide case-based examples.
In this webinar, the speaker discusses relevant clinical research ethical historical events, The Common Rule’s applications and definitions, and identifies ethical violations.
In this webinar, Dr. Micah Hester provides an overview of ethical historical events related to the practice of clinical research, summarizes the Common Rule, and discusses vulnerability and ways to respond to vulnerable situations. *ECHO ISPCTN Core Curriculum Module
