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.