GreenLight Clinical is a full-service Contract Research Organisation (CRO) with headquarters in Sydney Australia.
GreenLight can provide all the services required to take your product from first in man to regulatory approval and beyond. These include, amongst others, trial design, study management and monitoring, drug safety and pharmacovigilance, statistics, site selection, human research ethics committee (HREC) submissions, regulatory compliance, monitoring and reporting. We can also provide and host customised data management services including Electronic Data Capture (EDC). All of these services can be tailored to meet your expectations.
GreenLight Clinical's mission is to speed up the global development of safe and effective drugs while guaranteeing high standards of quality and ethics in clinical research.
Our experienced team of specialists can help you find the right patients and the right sites to support smooth completion of your global trials.