SPONSORS / CROs
SPONSORS / CROs

A reliable partner for the execution of clinical studies
CARE collaborates with Sponsors and CROs seeking a Center with experience, regulatory compliance, recruitment capacity, and consistent operational execution.
We provide a structure prepared to support each stage of the study, from feasibility to closeout, with a focus on data quality, smooth communication, and compliance with timelines.
We stand out for combining agile operations with responsible patient care, understanding that the study's final quality depends both on processes and on the clinical and human bond.

A reliable partner for the execution of clinical studies
CARE collaborates with Sponsors and CROs seeking a Center with experience, regulatory compliance, recruitment capacity, and consistent operational execution.
We provide a structure prepared to support each stage of the study, from feasibility to closeout, with a focus on data quality, smooth communication, and compliance with timelines.
We stand out for combining agile operations with responsible patient care, understanding that the study's final quality depends both on processes and on the clinical and human bond.

A reliable partner for the execution of clinical studies
CARE collaborates with Sponsors and CROs seeking a Center with experience, regulatory compliance, recruitment capacity, and consistent operational execution.
We provide a structure prepared to support each stage of the study, from feasibility to closeout, with a focus on data quality, smooth communication, and compliance with timelines.
We stand out for combining agile operations with responsible patient care, understanding that the study's final quality depends both on processes and on the clinical and human bond.
Institutional capacities
Quick and realistic feasibility
Agile studio activation
Active and sustained recruitment
Continuous clinical and operational monitoring
Document management and traceability
Preparation for audits and inspections
Direct communication with sponsors and CROs
Featured optional metric
Feasibility assessment time: 48 to 72 hours.
Tiempo de evaluación de factibilidad: 48 a 72 hs.
Institutional capacities
Factibilidad rápida y realista
Activación ágil del estudio
Reclutamiento activo y sostenido
Seguimiento clínico y operativo continuo
Preparación para auditorías e inspecciones
Comunicación directa con sponsors y CROs
Métrica opcional destacada
Tiempo de evaluación de factibilidad: 48 a 72 horas
Gestión documental y trazabilidad
Sponsors who trust CARE
Sponsors who trust CARE

























HOW WE WORK
HOW WE WORK
Our workflow is designed to provide predictability, operational speed, and quality control at every stage of the study.
01
Feasibility assessment
We quickly assess the protocol’s feasibility, the patient profile, operational capacity, and regulatory requirements to provide a realistic and useful response from the start.
01
Feasibility assessment
We quickly assess the protocol’s feasibility, the patient profile, operational capacity, and regulatory requirements to provide a realistic and useful response from the start.
02
Activation
We coordinate the study startup with an orderly and efficient approach, ensuring documentation, operational readiness, and preparation of the team involved.
02
Activation
We coordinate the study startup with an orderly and efficient approach, ensuring documentation, operational readiness, and preparation of the team involved.
03
Recruitment and tracking
We work with an active patient base and a referral network that support timely recruitment, while also maintaining a clear, professional, and personable follow-up experience.
03
Recruitment and tracking
We work with an active patient base and a referral network that support timely recruitment, while also maintaining a clear, professional, and personable follow-up experience.
04
Quality management
We apply standardized procedures, internal controls, and monitoring tools that help maintain data integrity, traceability, and readiness for audits and inspections.
04
Quality management
We apply standardized procedures, internal controls, and monitoring tools that help maintain data integrity, traceability, and readiness for audits and inspections.
05
Communication
We maintain direct, transparent, and timely communication with sponsors and CROs, prioritizing goal tracking and the agile resolution of operational needs.
05
Communication
We maintain direct, transparent, and timely communication with sponsors and CROs, prioritizing goal tracking and the agile resolution of operational needs.
Clinical Experience
Clinical Experience
Throughout our history, we have participated in studies related to various conditions, with particular experience in respiratory, allergic, dermatological, metabolic, and cardiovascular diseases.
