Time-stamped recording of the flowers, oils, edibles & beverages that a patient uses along with proprietary features to accurately measure onset/titration times and the optimal dosing for each patient’s individual needs.

Pending registration with Therapeutic Goods Administration (TGA) for a class IIa Medical Device to mitigate regulatory and auditing risks from our credible, independent & compliant software that monitors safety standards at scale for patients.

Credible RWE capabilities purpose-built as a patient-centred research and development tool to improve patient outcomes & strengthen business intelligence

Decentralised research tool that uses standardised patient assessments with a combination of qualitative and quantitative data to make it easier to undertake prospective and retrospective studies direct-to-patients.