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
Interested in Certara's biosimulation solutions? Want to speak to someone in our sales team? Click on the link below!
At Synchrogenix, Certara's regulatory writing consultancy, we know that the drug submission and approval process is more than just a series of stand-alone documents. With writers and editors worldwide, and experience in a range of therapeutic areas, functions, and document types, Synchrogenix provides strategic global regulatory writing support from pre-clinical through life-cycle management.
We have chosen to specialize because we believe regulatory writing is an expertise. The documents we create are an integral part of the drug development process and each program’s legacy. From development through project management to submission, we deliver the whole package.
By merging our cross-functional expertise with our writing experience, we deliver documents that not only support clients’ strategic messaging, but also enhance their marketability.