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