Steps for the implementation of the global seamless eConsent solutions

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Steps for the implementation of the global seamless eConsent solutions

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Embrace different country strategies for eConsent Integrate eConsent in trial planning Optimize informed consent form digitization timelines Train and communicate Build a monitor advocacy program www.prorelixresearch.com

How to Embrace different country strategies for eConsent?

www.prorelixresearch.com Global regulatory environments are complex, with nuanced differences among regions, countries and local communities.
www.prorelixresearch.com It’s important to note that while electronic signatures on an ICF are not accepted by all agencies regulating clinical trials, flexible, feature-rich eConsent products can be customized to meet each site’s local laws and guidelines. Provision of eSignature, offline signature and print-to-sign options are all essential to ensuring trial participants, sites and sponsors gain the full benefits of eConsent.

To ensure long-term success of global eConsent adoption, sponsors must maintain a growing database of eConsent signature modality acceptance, highlighting appropriate practices country by country and region by region.

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www.prorelixresearch.com Such databases must be constantly updated with regulatory intelligence to prevent risk noncompliance, trial delays and a regression back to paper ICFs.
ProRelix Research is here for the timely execution of your projects! www.prorelixresearch.com

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