Clinical research, Phase II/III

•         Study  design
•         Development of multi-center trials
•         Medical monitoring
•         Evaluation of drug safety and efficacy
•         Support for submission for international product registration
•         Support  for data with respect to the cost-effectiveness
•         Interpretation of  study data
•         Writing  the final reports of a study
•         Preparation of articles for journal publications or conference presentations

    Medical advice, Phase IV

•         Design of comparative studies of marketed products
•         Marketing support
•         Support  for data with respect to the cost-effectiveness
•         Advice on commercial needs operating within ethical frameworks and   
          legal constraints
•         Indication of medical viewpoint on marketing strategy
•         Control of promotional materials
•         Lecturing on company training programs and external audiences