Scientific Consulting

  • Drug development (research consultancy)
  • Design of drug development plans
  • Design and writing of Phase I/II study protocols
  • Writing study reports
  • Safety and tolerability evaluation of studies
  • Selection of investigators and/or CRO for Phase I or Phase II Studies
  • Selection of contract manufacturers for IMP
  • Selection of monitors
  • Advice on quality management of research (facility)
  • Advice on implementing ISO 9000/ISO 9001
  • Advice/training in Good Research Practices: Good Clinical Practices & Good Laboratory Practices
  • Quality Assurance evaluation
  • Detection/evaluation of scientific misconduct and/or fraud