Clinical Trial Management – respected for our expertise in clinical trial management, we can assist with all aspects of this service including feasibility, clinical trial design, preparation and co-ordination of ethics and regulatory submissions, clinical trial site monitoring, tracking of trial progress, preparation of clinical trial and confidentiality agreements, site start up and close out. Read more...

Data Management – delivering expertise and excellence in electronic and paper CRF design, data entry, development of data management plans, data cleaning, coding of adverse events, medical history and medication and data listings. Read more...

Statistics – our highly experienced team of statisticians can provide statistical and biostatistical analysis, SAS programming, database setup, statistical input into clinical trial design, sample size calculations, and more. Read more...

Medical and Scientific Writing – an experienced team of PhD and MBBS writers can provide medical, scientific and academic writing including clinical trial protocols, Investigator Brochures, ethics submissions and informed consent documents, clinical trial reports, publications, promotional material (including presentations), and more. Read more...