Monitoring, Logistics and Quality Control
Infociencia has more than 40 clinical trial monitors (CRAs), specialized in conducting clinical trials for the pharma, biotech and medical devices industry, both domestic and International. The 60% of our team has 2+ years of experience.
Our Monitors are employed or long-term and exclusively contracted freelancers. They regularly attend in-house education courses and are informed by the latest literature. Infociencia performs annual ICH GCP exams for their CRAs and SCRAs to ensure highest working standard. Several senior monitors and CRA supervisors are furthermore certified by ACRPI.
Project Management
Infociencia has the resources to assemble a motivated, integrated team that will best suit the needs of both the study and the sponsor based on factors such as therapeutic experience and location. Through a sound team structure, close communication, and detailed tracking and measurement, our Project Management group delivers consistently high quality for our clients.
- Coordinate all functional areas related to a study
- Maintain close communication with sponsors and sites
- Manage patient enrollment
- Provide ongoing quality measurement and control
- Manage the provision of timely data delivery
- Track projects through an integrated workflow system
- Develop risk management plans that include proactive solutions to potential difficulties
- Track and manage study budgets
We provide also Quality Audits for your clinical trials, and Training Programs for your CRAs
To learn more about this service, please contact us at masinformación@infociencia.com