Our full range of services includes the following:

• Project Management

• Clinical monitoring and site management

• Regulatory Affairs                  

• Feasibility & site selection

• Informed consent development          

• CRF design

• Study file setup           

• Site contract and budget negotiation

• Investigator meetings organization

• Translation and validation of study documents

• Medical writing and documents development consultancy

• Study Site Coordination

• Quality Management   

• Statistical analysis

• Medical Monitoring