• ACRO has established a standardized budget for the conduct of clinical trials. Budgets based on procedures and patient enrollment are linked to accounting system for accurate tracking and invoicing for payments and distribution.
  • ACRO has complete facilities including all necessary equipment for secure storage of study drug, study samples as well as all study documents.
  • ACRO will review and negotiate CTA’s respect of the sponsor and the University
  • ACRO will assist the sponsor in the EC approval of protocol, informed consent and all other documents required by the EC.

The Clinical Research Unit provides a facility for the conduct of clinical trials and other clinical research. The facility includes a complete array of equipment required to conduct First Time In Man as well as standard Phase I/BE projects. The teams have the expertise and facilities to perform the trials, evaluate the data and complete the final reports