The process of organising and analysing clinical trial data, then reporting key results based on the core objectives of the trial, requires dedicated expertise. Our leading team of statistical programmers, one of the largest in the UK, has considerable experience and knowledge of most therapeutic areas, together with the ability to deal with the complexity of various study designs.
To support your successful regulatory submission Synergy will utilise the project budget efficiently, assign adequate resource, and expedite the reporting efforts, either by working directly on your systems and implementing your Standard Operating Procedures (SOPs) or working procedures, or by managing the whole project in-house.
With more than fifty specialists based in London supported by a network of field and client-based experts throughout Europe and the USA, we are a reliable biometric resource. Two-thirds of us have more than five years’ experience in the industry, covering more than fifty therapeutic areas such as oncology, neurology, anti-infectives and respiratory.
We have proven expertise of statistical programming across all four phases of clinical development, through to the delivery of integrated safety and efficacy summaries for submissions to regulatory authorities.
As well as regularly undertaking full-service studies, we also provide support to in-house departments and work in tandem with off-shore teams, either on customers’ premises or our own.
Our services include: