ComplianceOnline

Issues related to informed consent in clinical trials

Instructor: Sarah Fowler Dixon
Product ID: 705453
  • Duration: 60 Min
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Read Frequently Asked Questions

This webinar will discuss some common literacy trends, issues with consent documents and tips to enhance the consent process.

Why Should You Attend:

According to current statistics, more than 90 million people in the United States have a hard time understanding and using health information. This is as many people as there are in France, Belgium and the Netherlands. To respond to this growing needed, President Obama signed the Plain Writing Act of 2010 and two other executive orders to cover the use of plain language. Use of Plain Language gets researchers closer to the historically used 6th to 8th grade level as the target for written consent documents. There are other tips as well that can improve the readability and acceptably of a consent document.

45 CFR 46 and 21 CFR 50 both require informed consent documents for research participants. Studies that are FDA governed will predominately use a written consent document.

This webinar will provide information to help improve written consent documents and consent processes.

Areas Covered in the Webinar:

  • Information on health literacy
  • Plain writing
  • Consent as a process
  • Increasing readability
  • 6 – 8th grade examples
  • Exculpatory language
  • Tips for using consent templates
  • What IRB reviewers like and dislike

Who Will Benefit:

  • Principal Investigators / Sub-investigators.
  • Clinical Research Scientists (PKs, Biostatisticians)
  • Safety Nurses
  • Clinical Research Associates (CRAs) and Coordinators (CRCs)
  • Recruiting Staff
  • QA / QC Auditors and Staff
  • Clinical Research Data Managers
  • Human Research Protection Professionals
Instructor Profile:
Rachelle D Souza

Sarah Fowler-Dixon
Education Specialist, Washington University

Dr. Sarah Fowler-Dixon, PhD, CIP is Education Specialist and instructor with Washington University School of Medicine. She has developed a comprehensive education program for human subject research which has served as a model for other institutions. She crafted budgets, policies, procedures, reporting, and training for the new program. She has initiated the planning, development, authorship and implementation of many human subjects’ research policies, practices, guidelines, submission and reviewer forms often working with state and federal authorities. She has provided consultation regarding ethical, federal, state, and institutional requirements for faculty and staff both in the design and execution of their projects and teaches research ethics and regulatory affairs and the fundamentals of research management to graduate and undergraduate students. More recently, she led a task force in the development of the Community Engaged Research Program at Washington University.

Dr. Fowler-Dixon has simultaneously served as an Independent Consultant, providing expertise and creating supplemental educational materials, including a copyrighted workbook. Prior to joining Washington University, she was the Educational Development and Learning Specialist for Saint Louis University serving on various committees to improve research, procedures, community outreach, and retention.

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Refund Policy

Registrants may cancel up to two working days prior to the course start date and will receive a letter of credit to be used towards a future course up to one year from date of issuance. ComplianceOnline would process/provide refund if the Live Webinar has been cancelled. The attendee could choose between the recorded version of the webinar or refund for any cancelled webinar. Refunds will not be given to participants who do not show up for the webinar. On-Demand Recordings can be requested in exchange.

Webinar may be cancelled due to lack of enrolment or unavoidable factors. Registrants will be notified 24hours in advance if a cancellation occurs. Substitutions can happen any time.

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