Support participation
Provide relevant information, question-level assistance and multilingual interactions across supported workflows.
For pharma & life sciences
Research grounded
in people's
lives.
Connect research participation with people's ongoing experience of care.
Configure consented, multilingual interactions and longitudinal information collection around a defined programme, population or research purpose.
Start with a focused survey or participant experience, with shared foundations that can support the next stage.
From participant engagement to understanding
A useful relationship.
Over time.
People bring experience, circumstances and priorities that add context to structured information. Carecircle provides configurable ways to capture and understand that context.
Collect what matters
Configure surveys and structured assessments, including patient-reported outcomes and experiences, with study-specific instrument and scoring requirements agreed for the programme.
Understand change
Bring participants’ responses and authorised history together to understand how their experiences change over time.
Connect care and research
Enable consented information and participation to support appropriately governed research, service learning and improvements in care.
Illustrative programme
One purpose.
Connected participation.
A programme wants to understand how people experience care over time, using structured questions and their own accounts.
- 01Define the research purpose
Agree the protocol, participant experience, consent and permitted uses.
- 02Configure the interactions
Shape questions, language content, support and relevant collection requirements.
- 03Build information over time
Build a consistent record over time, within the programme’s agreed purpose and governance.
- 04Learn with appropriate access
Use authorised information for the defined research or service-learning purpose.
Illustrative configuration. The protocol, access model and any specialist components are established for each programme.
Trust supports the relationship
Person-owned.
Purpose-led.
Consented.
Information belongs to the person it relates to.
Participation is voluntary. The purpose, consent requirements and appropriate access are defined for the programme, with permissions governing how information is shared and used.
Carecircle provides shared identity, relationships, records and interaction capabilities. Your programme defines the research requirements and the governance around their use.
Start with the need you have now
A survey. A programme.
A wider connection.
A focused tool can be a complete starting point. Extend into further interactions, populations or care and research settings when they serve your purpose.
The same foundations remain available as the configured experience grows: identity, person-owned information, consent, communication and governed workflows.