Centralized Clinical Data Sciences
Centralized Clinical Data Sciences provides the optimal outsourcing model. It further develops strategic alliances and functional outsourcing and allows for easy combining of data from different studies within and across Phases. Many Sponsors prefer to use different clinical vendors, based on therapeutic or geographic capability, but centralize clinical and safety data with us.
A centralized approach to Clinical Data Sciences brings peace of mind for sponsors trying to keep track of their data. For companies who seek to sell product licenses prior to market authorisation, or to co-develop a product, having the data all in one place and in a standard format increases the intellectual property value. Quanticate’s emphasis on standardization, re-use of existing material and team continuity has the added benefit of reducing the cost of clinical data management, biostatistics, statistical programming, medical writing and pharmacovigilance services.
Quanticate’s statistical consultancy team provide the guidance required in clinical trial design to achieve a successful outcome to your clinical trial programme. A core component of centralized clinical biometrics is our expertise in achieving economical and robust study designs, simulating the likely outcomes of studies under different scenarios, and support with regulatory bodies. The team can also offer advice in novel areas such as adaptive design methodology. Applying the correct methodology in statistical analysis that reflects actual trial conduct is another key component to ensure the clinical objectives of each clinical trial and programme of trials are met.
