PATIENT CENTRIC PLATFORMS

Challenges Addressed

• Significant time is required to set-up, customize and connect independent platforms for trials
• Significant time is lost to manage and transfer data across platforms
• The existing platforms are likely to be rigid and cannot integrate new stakeholders (e.g., physicians, nurses) to be on the same platform
• New functionalities are added with significant investment

Users

• Patients
• Clinical Study Team
• Multi-disciplinary team at the provider
• Health Care Professionals
• Care givers (based on Patients' consent)
• Additional stakeholders can be added simply
• Clinical Research Organizations

Applications

All platforms can be purchased stand-alone and combined with each other

• Patient Management & Engagement Platforms
• Nurse Education and Relationships Management Platforms
• Real-World Late Phase Evidence Generation Study - PRO Generation Platforms
• Patient Engagement and Retention Platforms
• Clinical Study HCP Education & Engagement Platforms

Note: all the platforms are "white label" and are branded with your company's / organization's brand.

Benefits

Gain Productivity

• Quickly customize (e.g., 1 - 2 days) and deploy purpose specific platforms that are specific to study
• Reduce deployment time, focus energy on getting the clinical trial operations running rather than customizing technology
• Manage all study platforms from a central place

Reduce Cost

• Gain savings - Reduce technology investment and patient generated data collection cost
• Gain time in start-up phase of clinical trials/ real-world studies
• Retain patients at low cost

Improve Patient Adherence & Compliance

• Retain patients on treatments as long as it is medically meaningful

Main Features

Manage Clinical Study Subject Population

• Get web-based patient consent
• Create dedicated platforms for each clinical / real-world study in 1-click
• (Optional) Dedicate 1 platform per patient - recommended for long term follow-up
• Transfer patient profile and records from one study to another
• Store screened-out patients for potential observational studies, transfer profiles if patients consent
• Manage access rights per stakeholders

Engage and Educate Patients

• Share multi-media content
• Send notifications triggered by events (e.g., reminders for physicians visits)
• Escalate cases, automatically triggered by the system (e.g., to a call center)
• Connect patients with relevant stakeholders (physicians, care team, etc.)
• Send key milestone reminders
• Collect Real-World Data & PRO (Patient Reported Outcomes)
• Ensure web-based quality control: Provide training and instructions for patients for self-administered PRO instruments
• Gather all treatment related reasons for patients failing to report at scheduled times or withdrawing from a treatment or clinical trial
• Implement how patient-level missing data will be handled during PRO collection process
• Implement rules for handling missing data/missing data imputation, that are determined during the PRO instrument development process
• Implement needed statistical analysis based on the protocol

Educate Patients on Disease and Study Protocol

• Collect evidence from patients in real-time on an ongoing basis

Reports & Analytics

• Provide custom analytics and reporting across all running platforms and for each study in real time or at pre-specified intervals

Direct-to-Patient Payments (Optional)

• Pay the patients directly when PROs are completed (if allowed and approved by your sponsors)