CRO

Our services

Effice Servicios Para La Investigación offers the monitoring services of phase I to IV clinical trials, post-authorization studies, research projects, real-world evidence studies (RWE) with highly qualified and trained personnel, which has solid experience in conducting clinical research protocols with a unique mindset in the market.

Effice manages monitoring services (face-to-face and remote) according to the ICH standards of good clinical practice, legislation, protocol, standard operating procedures and monitoring plan, offering its experience and flexibility to adapt to the needs and characteristics of each project. These services may include:

• Site Selection.
• Feasibiliy 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 and analysis.
• Communication with CEICs and Regulatory Agencies.
• Training of researchers and research staff.