Making electronic informed consent easy – in any language
Clinical Trial sponsors must ensure that participants understand key information, including the trials’ possible risks and benefits. Traditionally, gaining informed consent has been a challenging manual process. Complicated by complex scientific language and long forms resulting in reduced compliance and increased trial withdrawal.
Informed consent is much more than obtaining a handwritten signature, it’s a comprehensive process sponsors must undertake, providing relative information about the study. Information which will allow trial subjects to make an informed decision about whether or not they want to participate in the study.
Electronic informed consent (eConsent) refers to the use of electronic system and processes engaging prospective trial participants with interactive media to share relevant trial information, to obtain their informed consent remotely, share updates rapidly, allowing sponsors to collect higher quality data.
Download our brochure to learn more below about how RWS can make devising a superior multilingual eConsent platform easy!