Grand Pacific CRO’s highly trained statisticians are experts in producing high quality data analyses and reporting for clinical trials. As a part of a full service CRO, our statisticians work closely with the data management team to provide an integrated and seamless data solution. Our extensive knowledge and experience, combined with advanced therapeutic and regulatory expertise, provides confidence to the Sponsor.

Our services are flexible and tailored to your requirements from the initial stage of study design planning to final stages of data analysis and interpretation. All analyses are performed to ICH GCP standards using up-to-date high-quality software, including industry-standard SAS software. We use systems and procedures to avoid many of the difficulties typically encountered in research collaborations, ensuring your analyses are completed accurately and in a timely manner.