3 Major Regulatory Risks You Can Reduce With Electronic Informed Consent

Source: Signant Health

You may already know too well the challenges of a paper-based Informed Consent process, but did you know that Informed Consent is one of the most cited deficiencies by regulatory authorities? Paper-based informed consent increases your risk for delayed approvals, fines, litigation and even trial failure.

Register for our webinar if you are interested in understanding why these risks occur and how you can leverage electronic informed consent technologies to significantly minimize them. We've invited special guest speaker Sandra "Sam" Sathers to join CRF Health's Mika Lindroos as they discuss:

  • The status of regulatory risk in our industry
  • The 3 areas most at-risk in the current Informed Consent process
  • Solutions for reducing risk with eConsent
    ...And more!


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