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Informed Consent Forms for Data Sharing Scott Summers UK Data Service University of Essex Managing and Sharing Research Data: What is new with the GDPR? 4th May 2018Disclaimer The information provided
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Informed consent forms are used to ensure that individuals are fully informed about the risks and benefits of participating in a research study or medical procedure before agreeing to participate.
Researchers, medical practitioners, and healthcare providers are required to file informed consent forms for individuals participating in research studies or medical procedures.
Informed consent forms should be filled out by providing clear and comprehensive information about the study or procedure, including the potential risks, benefits, and alternatives.
The purpose of informed consent forms is to protect the rights and welfare of individuals by ensuring that they have all the necessary information to make an informed decision about participating in a study or procedure.
Informed consent forms must include information about the study or procedure, the potential risks and benefits, the individual's rights, and any alternatives available.
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