As an integral function within Biometrics, Quanticate programmers have supported clinical trials since 1994. Our programming team is the largest department within Quanticate and its global reach offers great flexibility for our customers. Experienced programmers have detailed knowledge of all Phases and all therapeutic areas across the drug development spectrum making them an ideal fit with existing project teams at client sites or to form the basis of new teams.

Programming takes a holistic view of clinical trials ensuring it dove-tails seamlessly with project team functions to deliver quality and excellence to meet our clients’ exacting requirements.

Whether we are using our internal global macro library, a client’s internal environment, or by

developing customized software solutions, Quanticate programmers are industry leaders in providing validated results to clinical study reports and submission ready deliverables.

By investing heavily in career development, we have built an adaptable workforce which monitors and adopts changing standards in both technology and the regulatory environment, enabling us to advise and guide our clients on the options available to them.

With an enviable track record of delivery, the programming department also looks to the future. Building on its core strength of SAS® Programming, we also offer support in electronic submissions, S-Plus® Programming and process development (including Software Development Life Cycle).