Clinical Research Services

Clinical Research Services

Our main services are:

• Feasibility Studies
• Consulting and assistance for the complete design of clinical research documents in compliance with International Good Clinical Practices (GCP’s), and Standard Operation Procedures (SOP’s)
• Project Planning
• Clinical Plan Development
• Site Identification and Assessment
• Regulatory Affairs
• Coordination of Investigational Sites
• Clinical Monitoring
• Medical Monitoring
• Quality Assurance
• Management of drug and laboratory samples
• Registration of new products / indications