eConsent for Complex Clinical Trials

As clinical trial protocols become more complex, patient informed consent forms and processes become more complicated as well. Not only is it critical to effectively engage patients in the consenting process early to ensure protocol adherence and meet trial milestones, it’s essential that their consent be tracked from initial screening through cohort or treatment group assignment and each subsequent amendment.
20 September, 2022 | 9am EDT 
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Why are cybersecurity risks to the healthcare industry so prevalent?

By 2025, global cybercrime will total $10.5 trillion, surpassing all other economies outside of the United States and China in size and profitability. Cybercrime in particular is having a significant negative influence on the American healthcare system. According to Earthweb, phishing emails are being sent out by cybercriminals daily from […]