Innovative solutions spanning global real-world data (RWD), technology, analytics and domain expertise enable confident decision-making and faster innovation.
Realize the full potential of your R&D investments
Get seamless, compliant, and secure access to research-ready RWD to support evidence generation across R&D and commercialization activities. Rich mastered data sets that include harmonized and integrated clinical, multi-omics, imaging, biomarkers, labs, EHR data and more inform even the most complex research and analysis – providing the reliable foundation you need for discussions with payers, regulators, and other key stakeholders across the entire value chain.
Shorten development timelines and accelerate speed to market
Securely access clinically-rich data spanning key markets around the world using RWD sourced from our global partner network. Or, let us help you manage and integrate your own or third-party data for efficient and seamless analysis. All enabled by a proprietary advanced technology platform that supports federated access, data management, and sharing in compliance with local regulations. Need help with protocol design, report writing, or data analysis? Our expert team can help with that, too.
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Draw on data from our proprietary catchment that includes 80 million+ patients from healthcare and research organizations around the world – Europe, Japan, APAC, and the Americas. We’ll apply your research objectives to identify, ingest, harmonize, and integrate the right data sources to ensure you’re set up for success from Day One.
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Get insights on your strategic areas of focus, including oncology, immunology, neurology and rare diseases, with structured and curated unstructured data. Includes demographic, clinical, imaging, and genomic data for a comprehensive view that supports a wide variety of use cases and regulatory requirements.
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Work with rich data sets, including multi-modal structured and unstructured elements, that are research-ready – harmonized, integrated and ready to apply to an array of advanced use cases. We can apply our data management standards to integrate data sets you provision, too, to enable an even more comprehensive approach.
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Have confidence that data access is well-managed, secure and in compliance with all local laws, including GDPR. Commission analyses or conduct your own in a built-for-purpose secure research environment tailored to your specific requirements – on premise or in the cloud. Federated options are also available.
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From initial design to final report publication, our experts can provide support for your team:
- Planning and executing clinical trials, including protocol development and statistical analysis plan (SAP)
- Data science services spanning epidemiology, biostatistics, and programming
- Medical and regulatory report writing
Support for a range of R&D and commercial needs
Whether you’re in clinical development, preparing for launch or assessing post-approval impact, tap into the world’s most extensive RWD to inform evidence-based decisions every step of the way. Enterprise or study-specific solutions available to support a range of needs.
Research & Development
Target population prioritization and characterization
Identifying subgroups of interest
Optimizing clinical trial design, inclusion/exclusion criteria
Natural history of disease
Regulatory Approval
Natural history of disease
Treatment pathways
Unmet needs
Identify suitable comparators
External control arm
HEOR Market Access
Burden of disease
Cost of illness
Health care resource utilization (HCRU)
External control arm (addressing varying standards of care)
Outcomes studies
Comparative effectiveness
Post Approval Follow Up
Outcomes studies
Comparative effectiveness
Uptake tracking
A trusted partner
For more than two decades, we’ve been the go-to partner to leading universities and academic hospitals, as well as top 20 pharma companies.
Learn more about BC Platforms
Contact us to discuss how BC Platforms can support your needs.