From the very first, C.RIS Pharma chose to be at the cutting-edge
Our Quality-Assurance program guarantees that all GLP-declared
studies are conducted according to the International standards of GLP.
Standard Operating Procedures (SOP) are kept updated and all study plans, critical study phases and reports are audited by the Quality-Assurance staff.
At C.RIS Pharma, the Quality and the Confidentiality are not only a
but a state of mind shared by all the team.