Our goal is to help our customers to design successful trials using modern statistical tool sets. We also conduct the analysis and the reporting of studies in a cost-effective manner. We are experts at translating data into usable information for decision making. Our services include:

• Statistical consulting

Protocol design

Clinical Study Reports (CSR) and publication support

Regulatory support

PK/PD modelling

• Statistical programming and reporting

SAS® programming and reporting using our in-house proprietary ClinXPORT® system

SAS® programming and reporting in your native SAS® environment

R programming

• Innovative software development designed for your needs validated and 21CFRPart 11 compliant
• FTE Resourcing

We manage approximately 40 clinical trial projects per year, spanning from phase I to phase IV of drug development, medical affairs support, cosmetics or medical device trials. We provide a range of ad-hoc statistical services for the design and analysis of your clinical studies, including:

• Phase I safety and pharmacokinetic studies
• Biomarker and proof of concept studies
• Dose-ranging phase II trials
• Phase III and regulatory submissions
• Post-registration phase IV
• Pre- and non-clinical trials

Benefit from our extensive pharmaceutical statistics experience to leverage the value of your clinical trials in a cost-effective way. We help you to optimize your R&D spending by designing the right study at the right time for the right cost.

We bring you modern statistical techniques such as Bayesian methods, adaptive designs, modelling and simulations to help you take better data-driven decisions. Our cost-efficient analysis and reporting capabilities using SAS® helps you build a solid information package to report study results, build registration dossiers, write publications or prepare interactions with investors.