Operational compliance is a "must" for all Oncacare research sites. Following our SOP's, Study visit worksheets and other operational guidance is regularly reviewed and monitored. Such consistent vigilance over the clinical research activity of sites minimises corrective actions later. Our clients are appreciative of our emphatic approach on this which is unique in the industry.
Oncacare’s principal aim is to deliver quality clinical trials data on time at every one of its investigator sites. Accurate patient data as well as our streamlined procedures comply with regulatory, ethical and ICH GCP requirements to achieve the best quality standards for our patients and our clients
We have developed high quality standard operating procedures (SOPs) which are strictly adhered to. We consider it vital to work with defined written processes to ensure that the quality of our clinical research is consistently high and delivered consistently across all our sites. Our investment in training to ensure practical adoption of these SOP’s is an ongoing and relentless priority.