Curavit Clinical Research
Virtual contract research organization focused on designing and executing decentralized and hybrid clinical trials with emphasis on digital therapeutics and connected devices. Services include decentralized trial protocol design and operational delivery, centralized virtual site operations, remote data capture and analytics, health economics and real-world evidence studies with claims/HIE linkage, diversity action plan implementation support, and regulatory/compliance support for digital-first studies. The company states use of HIPAA-aligned data stewardship and enterprise decentralized trial software and was founded in 2020 by clinical research and technology executives.
Industries
Nr. of Employees
small (1-50)
Curavit Clinical Research
Boston, Massachusetts, United States
Products
Virtual Clinical Site
An ideal solution for CROs, academic research institutions, and sponsors looking to run a trial with decentralized elements, integrating best-in-class tools to support scalable, efficient, and future-ready clinical research.
CRO Services
A full suite of services purpose-built for modern clinical trials, ranging from study design through FDA submission, supporting technology-forward, patient-centric trials.
Decentralized Clinical Trials
A virtual clinical trial service that eliminates the complexity of traditional trials with a central, virtual meta-site which accesses patients anywhere and monitors them remotely.
Inclusivity, Diversity, and Equity in Action (IDEA) Toolkit
Curavit's IDEA initiative is a comprehensive, step-by-step toolkit informed by FDA guidelines to optimize enrollment and retention of a diverse patient population from the very start of each clinical trial.
Phase II Hearing Loss Drug Trial Services
Decentralized and hybrid clinical trial services provided by Curavit Clinical Research for a Phase II pivotal trial involving sensorineural hearing loss treatment, focusing on data quality, protocol adherence, and remote monitoring.
Diverse Patient Recruitment
Removes barriers to access through personalized outreach, education, and diversity tracking for inclusive recruitment.
Virtual Clinical Site
An ideal solution for CROs, academic research institutions, and sponsors looking to run a trial with decentralized elements, integrating best-in-class tools to support scalable, efficient, and future-ready clinical research.
CRO Services
A full suite of services purpose-built for modern clinical trials, ranging from study design through FDA submission, supporting technology-forward, patient-centric trials.
Decentralized Clinical Trials
A virtual clinical trial service that eliminates the complexity of traditional trials with a central, virtual meta-site which accesses patients anywhere and monitors them remotely.
Inclusivity, Diversity, and Equity in Action (IDEA) Toolkit
Curavit's IDEA initiative is a comprehensive, step-by-step toolkit informed by FDA guidelines to optimize enrollment and retention of a diverse patient population from the very start of each clinical trial.
Phase II Hearing Loss Drug Trial Services
Decentralized and hybrid clinical trial services provided by Curavit Clinical Research for a Phase II pivotal trial involving sensorineural hearing loss treatment, focusing on data quality, protocol adherence, and remote monitoring.
Diverse Patient Recruitment
Removes barriers to access through personalized outreach, education, and diversity tracking for inclusive recruitment.
Services
Operation of a centralized virtual site to coordinate decentralized trial activities, remote participant engagement, scheduling, and distributed data collection.
End-to-end or modular clinical development services including protocol development, operations, monitoring, data management, and regulatory deliverables.
Study design and data integration to quantify health economic impact and longer-term outcomes, leveraging claims and HIE data for market access evidence.
Advisory support and operational tools to develop and implement diversity action plans, including situational analysis, culturally adapted recruitment materials, milestone setting and continuous enrollment monitoring.
Integration and management of third-party recruitment, laboratory, and enterprise decentralized trial software to create interoperable study technology stacks and streamline study start-up.
Centralized review, independent scoring, adjudication of recorded clinical assessments, remote source data verification, and targeted retraining to improve data quality and protocol adherence.
Operation of a centralized virtual site to coordinate decentralized trial activities, remote participant engagement, scheduling, and distributed data collection.
End-to-end or modular clinical development services including protocol development, operations, monitoring, data management, and regulatory deliverables.
Study design and data integration to quantify health economic impact and longer-term outcomes, leveraging claims and HIE data for market access evidence.
Advisory support and operational tools to develop and implement diversity action plans, including situational analysis, culturally adapted recruitment materials, milestone setting and continuous enrollment monitoring.
Integration and management of third-party recruitment, laboratory, and enterprise decentralized trial software to create interoperable study technology stacks and streamline study start-up.
Centralized review, independent scoring, adjudication of recorded clinical assessments, remote source data verification, and targeted retraining to improve data quality and protocol adherence.
Expertise Areas
- Decentralized and hybrid clinical trial management
- Virtual site operations for decentralized clinical trials
- Electronic data capture and eConsent/eCOA/ePRO implementation
- Digital recruitment and enrollment optimization
Key Technologies
- Electronic data capture (EDC)
- eConsent / eCOA / ePRO systems
- Telehealth and remote visit platforms
- Remote patient monitoring and wearable sensors
News & Updates
Industry event listing appearing on company site.
Company to oversee IRB submissions, site selection, data management, monitoring, clinical data capture selection, analytics, and CSR preparation for a US trial of a prenatal remote monitoring system.
Completed a decentralized trial for a wearable audiovisual device with remote outcome assessments, retention reporting, and remote ePRO/eCOA capture; data submitted for regulatory designation review.
Announcement of a dedicated health economics and outcomes research practice to support economic endpoints and claims/HIE data integration for trials.
Announcement of an IDEA toolkit to help sponsors develop and operationalize Diversity Action Plans for clinical trials, covering situational analysis, implementation strategy, content review, and ongoing optimization.
Press announcement describing company formation and mission to support virtual and decentralized clinical trials; includes founding team background.
Industry event listing appearing on company site.
Company to oversee IRB submissions, site selection, data management, monitoring, clinical data capture selection, analytics, and CSR preparation for a US trial of a prenatal remote monitoring system.
Completed a decentralized trial for a wearable audiovisual device with remote outcome assessments, retention reporting, and remote ePRO/eCOA capture; data submitted for regulatory designation review.
Announcement of a dedicated health economics and outcomes research practice to support economic endpoints and claims/HIE data integration for trials.
Announcement of an IDEA toolkit to help sponsors develop and operationalize Diversity Action Plans for clinical trials, covering situational analysis, implementation strategy, content review, and ongoing optimization.
Press announcement describing company formation and mission to support virtual and decentralized clinical trials; includes founding team background.