Electronic Informed Consent: Putting the Pieces Together for Implementation

As clinical trials have moved toward electronic methods for patient recruitment, trial management and data collection, the provision of candidate informed consent has remained a paper-based document that is increasingly outside the trial management process. More and more, the possibility of using electronic formats to enhance the consenting process is being considered. This audio conference examines the FDA guidelines for consent and their relationship to electronic consenting and inspection, as well as the importance of making connections to e-trial management and data capture.

In this presentation, our speaker outlines the steps to using electronic consent and gives examples of how electronic presentation of an informed consent document can increase candidate understanding and access to information. Dr. Brink also provides insight into making the e-consent decision, how to use e-consent to manage trial risk, and FDA guidance regarding e-consenting and its integration into the clinical trial process.

Electronic Informed Consent: Putting the Pieces Together for Implementation is being presented by Dr. Susan Brink, CEO, with ConsentSolutions, Inc. and airs on Thursday, March 18, 2010. For more details or to register, please visit our site at www.fxconferences.com

e-Consent: An Idea Whose Time Has Come

This presentation discusses the key elements to consider in implementing e-informed consent. Based on currently implemented online trial consents, crucial steps in the implementation process will be described.

Drawing from current national and international trial experience with electronic multimedia informed consent and the research literature on multimedia consent, presenters will discuss key lessons learned concerning subject and trial characteristics that impact on implementation of electronic consent and its’ success in a clinical trial. The session discusses a decision path for determining if e-consent can be effectively implemented for a trial.

e-Consent: An Idea Whose Time Has Come was presented by Dr. Susan Brink, ConsentSolutions, Inc. & Jovianna DiCarlo, Accugenex Technologies, Inc. and aired on 2008-12-03. For more details, or to download this event please visit our site at www.fxconferences.com

e-Consent: An Idea Whose Time Has Come

This presentation discusses the key elements to consider in implementing e-informed consent. Based on currently implemented online trial consents, crucial steps in the implementation process will be described.

Drawing from current national and international trial experience with electronic multimedia informed consent and the research literature on multimedia consent, presenters will discuss key lessons learned concerning subject and trial characteristics that impact on implementation of electronic consent and its’ success in a clinical trial. The session discusses a decision path for determining if e-consent can be effectively implemented for a trial.

e-Consent: An Idea Whose Time Has Come was presented by Dr. Susan Brink, ConsentSolutions, Inc. & Jovianna DiCarlo, Accugenex Technologies, Inc. and aired on 2008-12-03. For more details or to download this event, please visit our site at www.fxconferences.com