Clinical trials are by design, a scientific experiment, which require highly selective populations in a controlled setting, and with often
Real-world evidence (RWE) is increasingly being used within the regulatory and reimbursement process. RWE studies allow for a clearer understanding
A large global pharma company was required to run a complex global safety study by the regulatory authorities. This was
Baseline Plus provided the ideal platform to enable a specialised European Pharma company to run a post approval safety study
Cisiv’s electronic data capture (EDC) platform, Baseline Plus, is built specifically to meet the complex needs of post-approval research. Its
A leading global pharmaceutical company was looking for a fit-for-purpose technology and methodology to evaluate the effectiveness of an anti-psychotic
For years, the prospect of ‘virtual’ and decentralised research was discussed with hope as a potential disruptor to enable greater
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