For healthcare software partners
Add adverse-event reporting without becoming a PV company.
Your customers want safety reporting inside your product. Building it in-house means a compliance program of its own. VigilantLabs embeds it — via APIs and an integration pattern already proven in pharmacy dispensing software.
The integration approach
Embedded reporting APIs
Submit structured ICSRIndividual Case Safety Report — the standard record of one patient’s suspected adverse reaction to a medicine.s from your interface into VigilantLabs. You keep your UX; we handle case structure, coding and regulatory formatting.
Consent-based data flow
Patient and medicine details move only with recorded consent — the model we use in our Fred Dispense Plus integration.
Reduced clinical friction
Your users report without leaving your product or re-typing data. Adoption of the feature follows the workflow, not training sessions.
Compliance carried for you
The pharmacovigilance obligations — case quality, audit trail, regulatory submission — sit with the platform, not your roadmap.
A differentiator in tenders
ADR reporting is increasingly asked for in hospital and primary-care procurement. Ship it as a feature, win the question.
Local support for the partnership
Australian team, AEST/NZST hours, direct engineering contact during integration — not a ticket queue in another hemisphere.
Map the integration in one call.
Tell us about your product and where reporting would sit. We’ll sketch the API flow and the consent model on the first conversation.
Or call +61 425 228 763 · answered in Melbourne, AEST/AEDT