Our laboratories support the biotechnology industry in the development and approval of new products by delivering the laboratory component of clinical trials.
We achieve this through:
- Highly experienced and competent Laboratory personnel.
- Monthly Laboratory governance meetings.
- A robust and responsive internal Quality Management system which ensures the protocol requirements are met.
- The development of CTU specific SOP’s that can be used across CRS operations.
- Lab representatives are required to perform ongoing functional area specific risk assessment and provide feedback to the CTU Lab Lead which allows for risk mitigation planning and intervention prevention.