Medication adherence should not be a blind spot
Protocol adherence can influence how confidently trial teams interpret safety, tolerability and efficacy data. Delayed self-reporting may make it difficult to identify emerging adherence problems while a study is still underway.
How Wisepill supports clinical trials
- Objective medication-event information: Smart Pillbox openings provide a practical indication of medication access.
- Timely visibility: Review adherence patterns during the study rather than waiting for retrospective reports.
- Multi-site management: Organise participants, Smart Pillboxes, sites and user roles across a study.
- Data integration: Use structured exports and APIs to connect adherence information with trial databases and research workflows.
- Low-connectivity operation: Smart Pillboxes can store events and forward them when cellular coverage becomes available.
Built around each protocol
Wisepill works with sponsors, investigators, research organisations and implementation teams to configure Smart Pillboxes, platform workflows, reports and integrations around the needs of each study.