Why Choose The Clinical Register

 
THE CLINICAL REGISTER

About Us

We build a standards aligned registry that makes clinical research easier to register, easier to find, and easier to trust. Our focus is clarity, governance, and long term usability for investigators, institutions, journals, and ethics boards.

WHO ICTRP aligned CONSORT and PRISMA friendly Audit ready versioning Persistent IDs and clean citations

Our mission

Improve transparency and reduce research waste by supporting early registration, structured metadata, and evidence grade amendments. Every record is designed to be human readable and machine readable.

  • Make protocols discoverable and citable from day one

  • Support compliant reporting across trial and review workflows

  • Keep histories intact with versioned, auditable updates

What we do

A guided registration experience with validation for required fields, plus clean public pages that journals and research offices can rely on.

  • Structured record pages with persistent identifiers

  • Embargo controls and staged public release

  • Exports for citation and metadata reuse

Standards first
Mapped to WHO ICTRP minimum dataset with clear required field logic and structured schemas.
Governance and audit
Every amendment is versioned with a reason, preserving prior versions as citable records.
Global visibility
Clean pages, consistent taxonomy, and search friendly metadata designed for reuse.

How we govern records

Trust requires traceability. We separate public visibility from edit permissions and keep an auditable history of changes.

 
  • Role based access for investigators, sponsors, and institutional admins

  • Version control with change summaries and correction reasons

  • Embargo support with minimal public stubs where required

Governance details can be expanded in your Privacy Policy and Terms pages.

Who we serve

Built for busy teams who need fast registration without losing rigor.

  • Investigators registering trials, cohorts, registries, and reviews

  • Institutions tracking compliance and reminders

  • Journals and ethics boards verifying protocols and amendments

 

Build with transparency from the start

Register in minutes with structured fields, quality checks, and audit ready versioning that stays consistent as your study evolves.