Nonclinical

Nonclinical services

Holistic support is provided for clients/sponsors with those studies required before entering FIM/ early phase clinical trials. This might include pharmacology, safety and toxicology studies.

  • Assistance with planning, design, implementation, analysis and reporting of nonclinical studies
  • Expert report authoring
  • Identification and selection of the most suitable CROs
  • Monitoring of study progress
  • Conducting or supporting GLP audits