Clinical Research¶
Register clinical studies, manage subject enrollment (with an ethics‑approval gate), and record adverse events — using de‑identified subject codes for privacy.
Screenshot: Research dashboard — TODO
Medical → Research (/medical/research) shows total/recruiting studies, enrollments, and on‑study
subjects.
Studies¶
Research → Studies (/medical/research/studies) — register a study: title, phase (I/II/III/IV),
status (Draft / Recruiting / Active / Closed), principal investigator, description, enrollment
target, and the ethics‑approval reference (NHRC / ethics committee).
Enrollments¶
Research → Enrollments (/medical/research/enrollments) — enrol a subject with a unique subject
code, enrollment date, and status (Screening / Enrolled / On Study / Withdrawn / Completed).
Ethics approval gates recruitment
A subject cannot be enrolled into a study that has no ethics‑approval reference on file — recruitment is blocked until NHRC / ethics‑committee approval is recorded.
Adverse events / SAE¶
Research → Adverse Events (/medical/research/adverse-events) — record an adverse event against a
study subject: description, onset, severity, causality to the intervention, outcome, and
the ethics/NHRC reporting date. A Serious Adverse Event (SAE) is flagged for expedited
reporting and raises a critical alert so the obligation is visible. Onset and reporting dates
can't be in the future — the pickers cap at today and the server rejects a future date.
Privacy by design
Subjects are tracked by de‑identified codes (never names), and enrollment respects the patient's research consent.