Our Clinical Research Consulting Services
We have extensive knowledge and experience across the full range of biometrics, data management, analysis and reporting activities. We offer a wide range of services for individual clinical studies through to integrated databases and regulatory submissions support.
As authorized trainers in CDISC SDTM and ADaM, we provide training, hands-on support, and expertise about requirements, processes, and systems to support CDISC requirements. Our CDISC specialists are experienced in implementing standards for small, medium, and large pharmaceutical companies.
SAS & Statistical Programming are at the heart of the work we do at S-cubed. With our team of expert programmers, we have supported the global pharmaceutical industry since 2007. Our consultants can work on site or from our offices, you choose.
Our biostatistics team have a strong focus on accuracy and clarity, whilst still offering a tailored, collaborative service with a quick turnaround, allowing our clients to keep timelines and costs to a minimum.
Our Regulatory Affairs team have extensive regulatory expertise encompassing new chemical and biological entities, as well as medicinal products containing established active ingredients, generic compounds and therapies for orphan indications.
Visualise and explore your data using QlikView and Qlik Sense. We specialise in implementing Qlik tools for the Pharmaceutical industry. You will be able to optimise the speed and efficiency of your data analysis strategies, improving reaction time and reducing costs.
We provide only experienced Project Managers who have the knowledge, competences and expertise necessary to mitigate risks and create practical solutions. Our Project Managers are experienced in both small, large and multiple projects, and always do their best to integrate seamlessly with your existing team.