Factsheets
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ICH E6(R3) is now in effect. For biotech sponsors, that means active oversight requirements you can’t delegate away, ALCOA+ data integrity standards that legacy systems can’t meet, and site burden that affects enrollment and completion rates.
This one-pager covers how Castor’s unified platform — combining eConsent, eCOA, and EDC — addresses each of the three main ICH E6(R3) pressure points for biotech studies.
Inside: the specific guideline sections that matter, how Castor’s centralized monitoring handles them, and the expert team that configures it for you.
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