Requirements · Healthcare
ICH E6 Good Clinical Practice
2 Moraph products list it under “Requirements it supports”. The products support this requirement; meeting it remains your organization’s responsibility.
About the rule
What it is
ICH E6, Good Clinical Practice, is the International Council for Harmonisation’s guideline on the ethical and scientific quality standard for designing, conducting, recording and reporting clinical trials with human participants. Regulators including the FDA and the European Medicines Agency adopt it, and its third revision, E6(R3), was finalized in January 2025.
Source: ICH: Efficacy guidelines. This summary is for orientation only; read the rule itself or ask your counsel for what it requires of you.
Citations
How the products cite it
The exact wording on the product pages, with how many products use each.
- ICH E6 Good Clinical Practice 1 product
- ICH E6(R3) Guideline for Good Clinical Practice 1 product
For what it requires of your organization, read the rule itself or ask your counsel.
Products
The 2 products that support it
Clinical Trial Patient Recruitment App
Patient-facing mobile app for eConsent, retention, and adverse event reporting in trials.
Lists:
- ICH E6 Good Clinical Practice
Grant & Site Payment Manager
Automates financial reconciliation for research sites based on patient milestones.
Lists:
- ICH E6(R3) Guideline for Good Clinical Practice
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