SERVICES

Our services

Effice Servicios Para La Investigación offersa full range of clinical services for all types of studies including phase I, II, III and IV, post-authorization studies, research projects, and real-world evidence studies (RWE).

Clinical monitoring services are in-person and remote and in accordance with the ICH standards of good clinical practice, legislation, protocol, standard operating procedures and monitoring plan. We offer our experience and flexibility to adapt to the needs and characteristics of each project. These services may include:

• Site Selection
• Feasibility Studies
• Audits
• Site Initiation Visits
• Monitoring visits
• Close out visits
• Remote site management
• TMF management
• Investigational product management
• Query resolution
• Support for pharmacovigilance
• Data management
• Database design
• Online data collection notebooks
• Statistical design, programming and analysis
• Communication with Ethics Committees and Regulatory Agencies
• Training of researchers and research staff