Cromsource
ClinChoice is a full-service global contract research organization (CRO) established in 1995, dedicated to accelerating the development and commercialization of innovative drugs and devices. They provide comprehensive solutions across all stages of clinical development, post-marketing, and functional support, with a focus on making a positive impact on global healthcare. Their mission is to contribute to a healthier and safer world through innovative research and development.
Industries
Nr. of Employees
large (251-1000)
Products
Pharmaceutical Services
Outsourced services to the pharmaceutical industry specializing in clinical development and flexible resourcing solutions.
Medical Device Services
Expertise in medical device clinical trial services including regulatory strategy, submission, and clinical investigations in Europe and North America.
Biometrics Services
Biostatistics and biometrics services supporting clinical research and development.
Pharmaceutical Services
Outsourced services to the pharmaceutical industry specializing in clinical development and flexible resourcing solutions.
Medical Device Services
Expertise in medical device clinical trial services including regulatory strategy, submission, and clinical investigations in Europe and North America.
Biometrics Services
Biostatistics and biometrics services supporting clinical research and development.
Services
End-to-end clinical development including study planning, execution, monitoring, and close-out across phases I–IV.
Design and conduct of post-approval studies and real-world evidence generation to support lifecycle and market access objectives.
Monitoring regulatory changes, preparation of regulatory strategies, and support for regulatory submissions and interactions.
Biostatistics, data management, and generation of analysis-ready datasets for trials and regulatory use.
Safety case processing, reporting, and oversight for clinical and post-marketing programs.
Identification, qualification, and management of investigator sites across multiple regions to support recruitment and trial conduct.
End-to-end clinical development including study planning, execution, monitoring, and close-out across phases I–IV.
Design and conduct of post-approval studies and real-world evidence generation to support lifecycle and market access objectives.
Monitoring regulatory changes, preparation of regulatory strategies, and support for regulatory submissions and interactions.
Biostatistics, data management, and generation of analysis-ready datasets for trials and regulatory use.
Safety case processing, reporting, and oversight for clinical and post-marketing programs.
Identification, qualification, and management of investigator sites across multiple regions to support recruitment and trial conduct.
Expertise Areas
- Clinical trial management
- Post-marketing studies and RWE
- Medical devices and diagnostics development
- Oncology and hematology
Key Technologies
- Electronic data capture (EDC)
- Clinical trial management systems (CTMS)
- Real-world evidence analytics
- Biostatistical analysis