We are the disruptive force in clinical trial data. With deep data expertise, an advanced technology platform, and a flexible global model, Quartesian is the perfect fit for generics, small-to-midsize biopharma, and Phase I studies — as well as CROs who need the flexibility to add expert SAS resources on demand.
Choose Quartesian for clinical endpoint and BA/BE studies —we have a perfect track record of zero change orders.
All therapeutic areas. All trial phases. All you could ask for from your clinical data services company.
• Data Management
• Medical Writing
• Big Data Analytics
• Functional Service Provider (FSP)
And with 24/7 multinational help desk support, we always have your back.
Here’s why 3 of the world’s top 5 Generics firms (and many more) choose Quartesian for quality, speed, and low cost:
• Aggressive “First to File” track record and unmatched timelines
• BA/BE CDISC data conversion and Clinical Endpoint Studies
• Support for 380+ clinical trials over 2,000 sites across 20 countries
• Predictable & affordable budgets that Generics need
• CDISC Gold Member with proven expertise meeting new CDISC requirements
To learn more, visit quartesian.com.