The Orphan Reach Quality Management System defines the processes required to deliver a Quality Service. It is reviewed and updated continually in order to improve the effectiveness and efficiency of the business enabling us to consistently meet the needs and expectations of our Clients and Regulatory bodies.
• Our procedural documents provide the standards for conducting clinical trials from start-up through to close-out.
• Quality checks are built-in at each critical step of the trial, including TMF reviews, to guarantee high-quality outputs.
• Risk assessments are conducted, potential problems anticipated and steps taken to avoid them – the CAPA process is there, in support, should any significant issues occur.
Orphan Reach is committed to working to high standards across the board, thereby providing Quality results for our Clients.