Informed consent plays a very important part in any research project. It is very important that individuals who participate in research should do so voluntarily by understanding the purpose of research, its risks and potential benefits, as fully as rationally possible.
It is necessary to understand the standard elements of the informed consent document and the process involved while seeking informed consent from different individuals
Our expert presenter Dr. Nagina Parmar will provide you expert tips and strategies on strengthening your informed consent process as well as the elements of actual consent in the adult and pediatric populations. With the help of powerpoint presentation and references, you get a complete rundown on the principles, elements and challenges involved in the informed consent process and the related documentation.
Here’s just a sample of what you’ll learn:
Who should attend? Principal Investigators, Study Coordinators, Research Nurses, Senior Clinical Research Associates(CRAs), Clinical Research Project Manager, Clinical Research Associates
Dr. Nagina Parmar is a certified clinical research professional and senior clinical research Associate at the Hospital for Sick Children in Toronto. Dr. Parmar is also involved in teaching Biology, Microbiology, Life Sciences for Clinical practice, Principles of clinical research undergraduate and graduate courses at Ryerson University. She has published more than 30 journal articles and reviews in various national and international journals. Currently, she coordinating various Phase I, II...
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