Registration protects patients and the record of science
When plans and outcomes are captured up front, it becomes much
harder for selective reporting, silent outcome switching, or
undisclosed protocol changes to erode trust in the evidence.
A well-structured registry entry also becomes a shared reference
point for investigators, sponsors, ethics boards, and journals
throughout the life of the study.
}
title="Global visibility"
text="Help clinicians, patients, and systematic reviewers discover your work in seconds."
/>
}
title="Locked-in intent"
text="Pre-specify primary outcomes and analysis plans to anchor later reporting."
/>
}
title="Meta-analysis ready"
text="Provide structured fields that map cleanly to PRISMA and evidence synthesis tools."
/>
}
title="Institutional memory"
text="Give departments and sponsors a live view of active and completed studies."
/>
);
}
function ValueCard({
icon,
title,
text,
}: {
icon: React.ReactNode;
title: string;
text: string;
}) {
return (
);
}
function ComplianceGrid() {
const items = [
{
label: "ICMJE & major journals",
detail:
"Most high-impact journals require prospective registration for interventional trials.",
},
{
label: "Ethics boards and REBs",
detail:
"Many REBs now request a registry ID before approval or at first patient enrolment.",
},
{
label: "Funders & sponsors",
detail:
"Grant bodies and industry sponsors increasingly embed trial registration into contracts.",
},
{
label: "Systematic reviewers",
detail:
"Unregistered or poorly registered studies are harder to include in formal synthesis.",
},
];
return (
Registration has become a compliance baseline
The Clinical Register is designed to satisfy the expectations of
journals, ethics committees, regulators, and funders in one place.
{items.map((item) => (
))}
);
}
function StakeholderTabs() {
return (
What registration means for you
Different roles see different benefits. The Clinical Register gives
each stakeholder a clear, auditable view of the study.
