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Clinical Register

Standards-aligned clinical research registry — register, discover, and govern studies with audit-ready records

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Custom SystemsWeb Development

About the client

The Clinical Register is a modern platform for registering clinical research and making protocols findable, accessible, and auditable — built and hosted by Websight at clinicalregister.com. It aligns with WHO ICTRP requirements, supports CONSORT/PRISMA workflows, and gives investigators, ethics offices, and journals structured records with persistent IDs and metadata exports.

From the platform

Homepage — register, discover, and govern clinical research with WHO ICTRP and CONSORT/PRISMA alignment.
Homepage — register, discover, and govern clinical research with WHO ICTRP and CONSORT/PRISMA alignment.
Registry preview and KPIs — live search, registered studies, countries, compliance checks, and monthly visits.
Registry preview and KPIs — live search, registered studies, countries, compliance checks, and monthly visits.
Browse and register — advanced filters by specialty and a guided, standards-aligned registration workflow.
Browse and register — advanced filters by specialty and a guided, standards-aligned registration workflow.
Why The Clinical Register — standards-first design, governance and audit tooling, and global visibility with persistent IDs.
Why The Clinical Register — standards-first design, governance and audit tooling, and global visibility with persistent IDs.

What the platform delivers

Built for investigators, ethics coordinators, and research offices who need registration that is rigorous, transparent, and easy to use.

Standards-first registration

WHO ICTRP-aligned schemas, required-field guards, and automated quality checks — including the WHO 24-item minimum dataset.

Browse & discover

Filter by condition, intervention, phase, sponsor, registration status, and geography — with citation and JSON exports.

Governance & audit trails

Immutable audit history, role-based access, and versioned amendments — prior versions stay citable while the latest record stays canonical.

Guidance & visibility controls

Step-by-step guidance for interventional trials, observational cohorts, and manuscript citations — plus public or time-limited embargo options.

01

The challenge

Clinical study registration was fragmented — investigators lacked a single standards-aligned workflow, ethics boards needed auditable version history, and journals expected findable records with WHO-compatible metadata.

02

What we built

We built The Clinical Register end-to-end — guided registration with WHO 24-item minimum dataset validation, browse and advanced search, ORCID/DOI integration, amendment versioning with audit trails, public and embargoed visibility options, and practical guidance for investigators and research offices.

03

The outcome

A live registry at clinicalregister.com — standards-first records with compliance checks, citation-friendly study pages, and governance tooling that meets journal and ethics board expectations.

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