Palleos Healthcare
Palleos is a dedicated CRO that has been crafting solutions for clinical studies in Europe since 2005. With a focus on efficiency and care, Palleos offers extensive expertise across 29 therapeutic areas, supporting over 420 projects and enrolling more than 74,580 patients. The company operates across 18 countries in Europe, providing comprehensive services in clinical management, biometrics, and consulting, aiming to reduce drug development timelines and facilitate access to global medicine.
Industries
Nr. of Employees
small (1-50)
Products
CRO services for
Tailored CRO services spanning from product development to the design and conduct of tailored trials for marketing authorization and expansion for small to midsize biotech companies.
Palleos CRO services for Pharma
Full-service contract research organization solutions specialized for clinical trials across Central and Eastern Europe for the pharmaceutical industry.
Palleos CRO services for Medtech
Tailored solutions to navigate Medical Device Regulation (MDR) complexities, develop strategies for market authorization, and conduct clinical investigations.
Clinical Study
Comprehensive clinical study management services provided by Palleos Healthcare, including project management, site management, and monitoring services to ensure compliance and efficiency.
Clinical Study Design Preparation
Clinical trial design and planning to anticipate risks and optimize studies for efficient and reliable results.
Regulatory Writing
Compliant and comprehensive medical writing services ensuring accurate, transparent, and clear communication with health authorities.
CRO services for
Tailored CRO services spanning from product development to the design and conduct of tailored trials for marketing authorization and expansion for small to midsize biotech companies.
Palleos CRO services for Pharma
Full-service contract research organization solutions specialized for clinical trials across Central and Eastern Europe for the pharmaceutical industry.
Palleos CRO services for Medtech
Tailored solutions to navigate Medical Device Regulation (MDR) complexities, develop strategies for market authorization, and conduct clinical investigations.
Clinical Study
Comprehensive clinical study management services provided by Palleos Healthcare, including project management, site management, and monitoring services to ensure compliance and efficiency.
Clinical Study Design Preparation
Clinical trial design and planning to anticipate risks and optimize studies for efficient and reliable results.
Regulatory Writing
Compliant and comprehensive medical writing services ensuring accurate, transparent, and clear communication with health authorities.
Services
Full-service management of interventional and non-interventional clinical trials across Phases I–IV and multiple therapeutic areas.
Statistical planning, analysis and statistical programming services for clinical trials.
Clinical data management services and implementation/advisory for CTMS, EDC and data integration from digital sources.
Regulatory strategy, submission support and guidance on EU regulatory systems and medical device regulation.
Site feasibility evaluations, start-up planning and risk identification to accelerate trial initiation.
Design and conduct of studies using remote monitoring, wearable devices and ePRO solutions.
Full-service management of interventional and non-interventional clinical trials across Phases I–IV and multiple therapeutic areas.
Statistical planning, analysis and statistical programming services for clinical trials.
Clinical data management services and implementation/advisory for CTMS, EDC and data integration from digital sources.
Regulatory strategy, submission support and guidance on EU regulatory systems and medical device regulation.
Site feasibility evaluations, start-up planning and risk identification to accelerate trial initiation.
Design and conduct of studies using remote monitoring, wearable devices and ePRO solutions.
Expertise Areas
- Clinical trial management
- Biostatistics and statistical programming
- Clinical data management and eClinical systems
- Patient recruitment and enrollment optimization
Key Technologies
- Clinical Trial Management System (CTMS)
- Electronic data capture (EDC) / eCRF
- ePRO systems
- Wearable device data integration