Qualified eSignature in Electronic Consent Systems – A Primer for Clinical Trial Professionals

Electronic consent (eConsent) systems have proven to add value to patients, sponsors, and sites. However, varying regulations across regions and countries can impact implementation of eConsent solutions and dilute the benefits. How can clinical trial professionals adapt a global approach to eConsent rollouts that accounts for these differences?

Join IQVIA Technologies for an informative webinar on electronic signature (eSignature) technology for eConsent. We’ll delve into global regulatory scenarios and options for meeting eSignature requirements in each scenario, including the benefits and limitations of:

– Print to sign
– Simple or Electronic Signature (SeS)
– Advanced Electronic Signature (AeS)
– Qualified Electronic Signature (QeS)

Learn what to look for in eConsent solutions to ensure you’re prepared for every trial.