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
Over 50,000 attendees across hundreds of companies have taken advantage of our easy-to-use audio conferences to stay abreast of a fast-changing business environment. We specialize in Life Science conferences, along with topics relevant for HR, Marketing, Legal, and Finance professionals. Come check out our library of past audio conferences and see what's upcoming at FXConferences
Showing posts with label ConsentSolutions. Show all posts
Showing posts with label ConsentSolutions. Show all posts
Monday, February 1, 2010
Friday, January 29, 2010
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
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
Wednesday, January 20, 2010
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
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
Wednesday, February 25, 2009
Leveraging Technology for Conducting More Efficient Trials in India
Compelling fundamentals are driving the growth factor of the clinical development sector in India. There is potential for innovation and sector transformation if technologies, processes and workflow can be leveraged to select quality sites that have the subject populations to meet enrollment goals and efficiently manage your clinical trial projects while enhancing the quality, regulatory and ethics training of clinical site research personnel. Are your clinical trial management processes well-suited for this clinical trials landscape? Increasing efficiency with costing and timelines is crucial to a successful trial, and there are an array of technologies available to help you achieve your clinical trial goals.
This audio conference will provide insights on technology, process and procedures to effectively manage clinical trials in India. You will be armed with the most efficient technology-based solutions mapped with workflow processes for continued success in the Indian pharmaceutical marketplace.
Leveraging Technology for Conducting More Efficient Trials in India is being presented on Wednesday, March 18th, 2009. For more details, please visit our site www.fxconferences.com
This audio conference will provide insights on technology, process and procedures to effectively manage clinical trials in India. You will be armed with the most efficient technology-based solutions mapped with workflow processes for continued success in the Indian pharmaceutical marketplace.
Leveraging Technology for Conducting More Efficient Trials in India is being presented on Wednesday, March 18th, 2009. For more details, please visit our site www.fxconferences.com
Monday, February 2, 2009
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 on 2008-12-03 and is available for download at www.fxconferences.com
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 on 2008-12-03 and is available for download at www.fxconferences.com
Wednesday, November 12, 2008
e-Consent: An Idea Whose Time has Come
This presentation will discuss 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 will discuss a decision path for determining if e-consent can be effectively implemented for a trial.
e-Consent: An Idea Whose Time has Come is presented by Susan Brink, President & CEO, of ConsentSolutions, Inc. and Jovianna DiCarlo, President, of Accugenex Technologies, Inc. This audio conference airs on Wednesday, December 3rd 2008, for more details or to signup, please visit our site www.fxconferences.com
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 will discuss a decision path for determining if e-consent can be effectively implemented for a trial.
e-Consent: An Idea Whose Time has Come is presented by Susan Brink, President & CEO, of ConsentSolutions, Inc. and Jovianna DiCarlo, President, of Accugenex Technologies, Inc. This audio conference airs on Wednesday, December 3rd 2008, for more details or to signup, please visit our site www.fxconferences.com
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