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French SNDS Real World Data Solutions

Access Europe’s largest source of real-world data and design studies

Identify treatment patterns and patient outcomes, uncover unmet needs for rare disease populations, and better understand resource utilization in clinical settings.

Leverage unmatched SNDS database expertise
for RWE studies

The French National Healthcare Data System (SNDS) is Europe’s largest and most comprehensive healthcare database, covering over 65 million lives – approximately 99% of the French population. Certara is the first non-academic organization granted access to this anonymized dataset, enabling unparalleled real-world evidence (RWE) generation. Whether you seek to quantify unmet needs, demonstrate benefit/risk, or analyze treatment patterns, our expertise in SNDS empowers your strategic decisions.

Comprehensive reach

Gain insights from a database covering more than 99% of the French population, ensuring robust and representative data analysis.

比類のない専門知識

Leverage decades of experience in real-world studies and advanced SNDS analysis for precise outcomes.

Advanced analytical methodologies

Link observational studies to advanced modeling in access data platforms built for bridging to real life studies.

Optimal rare disease research

Effectively study small populations for rare disease research by taking advantage of the universal nature, size and long follow-up time characteristic of France’s SNDS database.

Real world solutions utilizing the French SNDS database

Evidence generation planning
Outcomes research and surveys
Burden of illness studies
Retrospective database studies
Chart reviews
Electronical medical record analytics

Why choose Certara for SNDS data analysis

As the first successful non-academic application for French SNDS database access, Certara delivers unmatched expertise in SNDS analysis and offers innovative solutions tailored to your specific needs. Our team of experts ensures that every study is designed to maximize data utility and minimize biases, leveraging the SNDS database’s unique attributes for impactful insights.

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20
Years’ experience in conducting observational studies in France.
200
Access to >200m patient lives through a diverse coalition of registry, claims and HER databases including French SNDS.

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Partner with Certara to access and analyze the French SNDS database. Our unparalleled expertise in real-world evidence generation ensures impactful results, from identifying unmet needs to evaluating treatment outcomes.

Over 65 million lives covered by SNDS.
Decades of experience in real-world studies.
Pioneers in advanced SNDS methodologies.

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FAQs

What makes the SNDS database unique?

The SNDS database covers over 99% of the French population, offering comprehensive and representative healthcare data.

How does Certara ensure data quality?

We utilize advanced methodologies and robust study designs to minimize biases and maximize data utility.

Can SNDS data be used for rare disease studies?

Yes, the SNDS dataset’s size and long follow-up periods make it ideal for rare disease and drug-related adverse event research.

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