Certara is the largest and most comprehensive provider of biosimulation (modeling and simulation), strategic pharmacometrics, and regulatory writing consulting services. Our multidisciplinary team works alongside clients to inform key drug development decisions and expedite the processes around achieving regulatory milestones.
Certara combines its industry renowned pharmacometric and regulatory consultants with our vast software portfolio to provide services that focus on specific outcomes, therapeutic areas, regulatory milestones, and specific populations.
United States: 1-888-708-7444 or 1-919-852-4685
France: +33 1 56 95 17 10
Germany: +49 89 45 10 300
United Kingdom: +44 (0) 114 292 2322
India: +91 984 500 6625
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Certara’s D360™ R&D data platform solves data challenges faced by scientists and IT staff throughout biopharmaceutical organizations by integrating and leveraging the large amount of diverse scientific data generated by sponsor companies and their outsourced partners to optimize crucial decisions. With D360, users can:
Get faster time to insight
D360 helps scientists get data easily and analyze and present it the way that they want. D360 users can analyze trends over past and ongoing studies to improve study designs.
Reduce IT overhead
With D360, scientists have self-service access to data and analytics freeing research IT staff from user support to higher value activities.
Support organizations of any size
D360 is a scalable solution from the largest pharma to the smallest biotech.
It supports both standard workflows like project data views and data mining to allow users to ask and answer scientific questions that were previously inaccessible.
D360 supports chemists, biologists and research managers alike in their use and interpretation of research data. Incorporation of logistical information such as compound inventory and access to notebook data in ELNs adds practicality considerations to research decisions. When asked about Certara’s scientific informatics solutions, a scientist in Biochemistry and Enzymology at Agios Discovery recalled that “What used to take us a huge amount of time plus about 50 more mouse clicks now takes one click in D360.” Learn how to gain efficiency with D360. Check out the brochure.
D360 provides preclinical pharmacologists, toxicologists, and pathologists with the ability to understand data at a level beyond an individual study. With D360, scientists can explore cross species exposure vs. toxicology, control group drift, and prevalence of adverse effects within drug classes. Learn why a D360 client who is a Pathologist in Toxicology at a Top 10 Pharma said, “It’s so cool that D360 lets me just ask the questions I want. All the tedious work is removed and I’ve been surprised at some of the things I’ve found in the data already.” Check out the brochure.
For the ultimate value, D360 can draw on both discovery and preclinical data sources to help answer questions that cross scientific domains.