Statistical programming in clinical trials is a vital component of all drug development. Whether you are a Large Pharma, Mid-size Pharma, Biotechnology, Device or Nutraceutical company, you will need to turn your validated data into interpretable information ready for biostatistical analysis.
Statistical Programming enables clinical trial reporting via the creation of regulatory submission ready analysis datasets and production of Tables, Listings and Figures (TLFs). These deliverables help you understand the safety and efficacy of your investigational product and the outcomes of your trial hypotheses.
Citrine Healthcare will rapidly resource any studies that you require additional support or expertise on so you can meet your regulatory approval milestones with submission ready deliverables.
Our statistical programmers will seamlessly integrate into your existing team or can form a whole new department depending on your resourcing requirements. Our programmers also work side by side our biostatistics department who have over 25 years of experience which enables us to provide you with additional statistical advise across your studies.
Citrine Healthcare strives towards
100% quality and 100% on time metrics as
part of our philosophy.
Citrine Healthcare strives towards 100% quality
and 100% on time metrics as part of
our Coded to Care Philosophy.
With programmers across several continents we are
well positioned to support customers
and studies around the globe.
You will have 24 hour access to our team
and constant responses to any
requirements you have.
Our expert programmers have detailed knowledge of all Phases and experience of a multitude of therapeutic areas across the drug development spectrum making them an ideal fit within existing project teams at client sites or to form the basis of new teams, forming long lasting partnerships.
