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

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Steps for the implementation of
the global seamless eConsent
solutions

2. 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

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Global regulatory environments are complex, with nuanced
differences among regions, countries and local communities.
How to Embrace different country
strategies for eConsent?

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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.

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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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Such databases must be constantly updated with regulatory
intelligence to prevent risk noncompliance, trial delays and a
regression back to paper ICFs.

7. ProRelix Research
is here for the
timely execution
of your projects!
www.prorelixresearch.com