ars® Drug Accountability

  • Administration of drug supply to the centres
  • Confirmation of drug receipt by study nurse or investigator
  • Registration of undelivered or damaged drugs in the course of the drug confirmation process. Immediate automatic information to the monitors by e-mail.
  • Administration of all study medications delivered to a study centre.
  • RDE supported handing out of study drugs according to protocol and randomization plan, especially if kind and amount of medication depend on further clinical parameters of the patient.
  • Permanent visualization of the status of study medication supported by colors, visible to investigator, study nurses, monitors and sponsor.
  • Detailed registration of return of unused study medication (including registration of the status of returned drugs, weight, number of units etc)
  • Registration of the collection of returned or unused medication by the monitors