Our Services

Design, Execution and Analysis of Bioavailability and Bioequivalence studies

We offer in patient facilities according to special needs in relation to bioavailability and bioequivalence studies. Working closely with experts, we offer highly qualified personal staff and specially dedicated study coordinators, internists, nutritionists, pharmaceutics, biochemists and nurses for the following services:

  • One or multiple doses.
  • First in human administration.
  • Drug-drug interaction.
  • PK in renal patients, PK in patients.
  • Bioavailability
  • Pilot studies for new pharmaceutical and new forms.
  • Food effects.
  • In vivo-in vitro relation.
  • Investigational Protocol design, CRF design and informed consent design.
  • Statistical plan, size sample calculation.
  • Interaction with ethical committees and local committees.
  • Subject recruitment.
  • Medical and lab exams, ECG, Rx.
  • Out patient follow-up.
  • Bio analytical and analytical quantification.
  • Adverse events registration and reports.
  • Electronic data capture.
  • Data statistic analysis and bioequivalence analysis.