FMD K&L
ClinChoice is a global full-service Contract Research Organization (CRO) dedicated to accelerating the development and commercialization of innovative drugs, devices, and diagnostics. With over 27 years of experience and a presence in more than 20 countries, ClinChoice provides comprehensive clinical development, post-marketing, and functional service support to pharmaceutical, biotechnology, medical device, and consumer health companies. The company is committed to high-quality service, innovation, and building enduring client relationships to contribute to a healthier and safer world.
Industries
Nr. of Employees
medium (51-250)
FMD K&L
300 Welsh Road, Building 5, Suite 201, Horsham, PA 19044, USA
Products
Data visualization and dashboarding product
A data visualization tool that provides customizable, real-time graphical representations of clinical and operational data to support program oversight and decision-making.
eClinical data capture and management platform
Deployment and integration of eClinical suites providing EDC, ePRO/eCOA, eConsent, SAE reporting and related trial management functions.
Custom eClinical solutions and enterprise IT services
Technology division services delivering custom eClinical integrations, enterprise IT platforms, and data science consulting for clinical operations.
Data visualization and dashboarding product
A data visualization tool that provides customizable, real-time graphical representations of clinical and operational data to support program oversight and decision-making.
eClinical data capture and management platform
Deployment and integration of eClinical suites providing EDC, ePRO/eCOA, eConsent, SAE reporting and related trial management functions.
Custom eClinical solutions and enterprise IT services
Technology division services delivering custom eClinical integrations, enterprise IT platforms, and data science consulting for clinical operations.
Services
Integrated program delivery covering clinical operations, biometrics, regulatory, safety, medical monitoring, and medical writing across the product lifecycle.
Provision of dedicated functional teams or individual specialists who integrate with sponsor SOPs and systems, available remote or on-site, with managed oversight options.
Statistical design and analysis, data management, CDISC/eSubmission support and statistical programming for clinical studies and regulatory submissions.
Safety case processing, adverse event reporting, pharmacovigilance system support and post-marketing safety activities.
Regulatory strategy, dossier preparation, local registration support and engagement with health authorities across global regions.
Custom eClinical platform deployment, data integration, visualization solutions, and analytics to support clinical operations and decision-making.
Integrated program delivery covering clinical operations, biometrics, regulatory, safety, medical monitoring, and medical writing across the product lifecycle.
Provision of dedicated functional teams or individual specialists who integrate with sponsor SOPs and systems, available remote or on-site, with managed oversight options.
Statistical design and analysis, data management, CDISC/eSubmission support and statistical programming for clinical studies and regulatory submissions.
Safety case processing, adverse event reporting, pharmacovigilance system support and post-marketing safety activities.
Regulatory strategy, dossier preparation, local registration support and engagement with health authorities across global regions.
Custom eClinical platform deployment, data integration, visualization solutions, and analytics to support clinical operations and decision-making.
Expertise Areas
- Clinical trial management
- Biostatistics and biometrics
- Clinical data management and standards (CDISC/SEND)
- Pharmacovigilance and safety surveillance
Key Technologies
- Electronic data capture (EDC)
- ePRO / eCOA
- eConsent
- eTMF
News & Updates
ClinChoice led a landmark full-service Phase III clinical trial involving over 600 adolescent patients with asthma across 16 countries and more than 150 sites worldwide.
An overview of recent updates to the FDA’s accelerated approval pathway, emphasizing the importance of confirmatory trials and regulatory compliance.
ClinChoice’s corporate social responsibility initiative in Armenia, planting thousands of trees to promote environmental sustainability.
Guidance on the standards for nonclinical data exchange and how ClinChoice supports compliance.
Recognition for leading respiratory clinical research with a large-scale international trial.
ClinChoice led a landmark full-service Phase III clinical trial involving over 600 adolescent patients with asthma across 16 countries and more than 150 sites worldwide.
An overview of recent updates to the FDA’s accelerated approval pathway, emphasizing the importance of confirmatory trials and regulatory compliance.
ClinChoice’s corporate social responsibility initiative in Armenia, planting thousands of trees to promote environmental sustainability.
Guidance on the standards for nonclinical data exchange and how ClinChoice supports compliance.
Recognition for leading respiratory clinical research with a large-scale international trial.