HospitalsAescia for Hospitals is an investigational Software as a Medical Device under the TGA Class IIa pathway. Not yet available for commercial supply.
ClinicsAescia for Clinics is a workflow and patient-preparation tool. It does not propose clinical decisions and is not a medical device.
We publish plainly. No press copy, no launch videos, no "we are thrilled" posts. Just dated entries when something real happened.
Dr Shuangbo Liu at St. Boniface Hospital in Winnipeg has won a St. Boniface cardiovascular seed grant, funded through the National Bank Cardiac Classic, for TPD-CONNECT. It is a 12-month study that co-designs and prototypes tailored post-discharge support for cardiac patients. Aescia is a named collaborator, configuring the platform and building the prototype. Dr Liu is the principal applicant and the work runs at St. Boniface.
Published an open surveillance-interval reference for clinicians. Enter what a colonoscopy found and it returns the recommended interval together with the wording of the guideline it came from, across six guideline sets covering the United States, Ontario, Alberta, British Columbia, Australia, and Europe. It runs in the browser, needs no account, and stores nothing.
SAFE-Discharge, a prospective single-centre evaluation of Aescia for Hospitals in adults recovering from cardiothoracic surgery, went live at the Royal Prince Alfred Hospital cardiothoracic surgical unit in June 2026. It is registered with the Australian New Zealand Clinical Trials Registry and sponsored by Sydney Local Health District.
Aescia has joined the Medical Technology Association of Australia's MedTech Compass program, which supports Australian medtech companies moving from concept to commercial adoption across regulatory, reimbursement, and clinical evidence.
Published the operating team, added trial-site and research-institute affiliations, unified the contact flow, and started this updates log. Clinic pricing stays explicit: no per-seat math.
The SAFE-Discharge trial at Royal Prince Alfred Hospital has cleared human research ethics review. Site-specific governance and IT assessments follow. No trial recruitment on this site; enrolment happens through the RPAH cardiothoracic unit under ethics approval.
Aescia joined the Product-Market-Fit programme at the CHEO Research Institute in Ottawa, with a paediatric-respiratory post-discharge pathway as the working focus. Four candidate specialties under evaluation inside the programme: paediatric respiratory, paediatric cardiothoracic adjacency, paediatric gastroenterology, and paediatric oncology.
Compiled a ten-document evidence base covering international guidelines, digital interventions, operational economics, diabetes and anticoagulant management, GLP-1, and special populations for colonoscopy preparation. Underpins the clinician-authored prep pathway going into design-partner pilots.
End-to-end walkthrough across patient, clinician, and admin flows. Pathway authoring, multichannel reminders, GLP-1 overlay, diabetic and anticoagulant scenarios, recall tracking, and structured export. Production deploy follows once production database and EMR integration targets land.
Application MVPV25RD3347 lodged with Investment NSW on 10 April 2026. Matched-funding programme for commercialisation work. Recipients are expected to be announced later in 2026.
Aescia participated in Concordia University's Beat the Odds hiring event through the District 3 Innovation Hub. The program connects Montreal students with early-stage startups; Aescia hired its first Beat the Odds intern through the initiative.
Aescia joined District 3, Concordia's innovation hub for bio, health, and high-tech startups. The programme provides coaching, mentorship, and access to Montréal's startup ecosystem.
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