Clinical Monitoring
Monitoring is one of our core competencies. We assure that all
monitors are sufficiently trained on individual study concepts. They can
rely on elaborated SOPs and innovative software solutions and will be
supervised throughout the study. With their monitoring reports they
contribute to up to date knowledge of your trial status at each
participating hospital.
Monitoring activities consist of
- Recruiting of Investigators
- Preparation and delivery of necessary documents to study sites
- Pre-study visits
- Site openings
- Monitoring visits
- Source data verification
- Closing-out visits
We conduct field monitoring to ensure protocol and regulatory compliance and timely submission of high-quality data. Datamanagement skills of our monitors ensure low query rates and successful cooperations with internal and external data management.
Algora delivers services and software for clinical research to industry and academic institutions.
- Clinical trials phase II-IV
- Non-interventional studies
- Investigator initiated trials
- Epidemiological research