As a CRO you need to service product life cycle development strategies of pharmaceutical and biotechnology companies and realign your own development strategies to new types of players and the needs of a growing range of constituents.
Clinical research has become a complex field that requires many areas of expertise which is not necessarily available “under one roof”. More and more CRO’s are partnering with specific parties to buy-in expertise so they can meet their clients and regulatory requirements.
ITREAS assists you to meet your timelines and enrolment targets.
ITREAS and its associates have partnered with CRO’s on a multitude of clinical trials and we are perfectly positioned to work with you in achieving the best results for your clients. We have worked with several of the worlds largest CRO’s, as well as small and medium sized organisations. Our fully ICH-GCP compliant “investigator friendly” processes ensure you to deliver a constant cost-effective flow of adjudicated safety and efficacy data. Our certified processes will feed all blinded adjudicated data in your data systems.
Our services, amongst others, include: