Sentence examples for monitoring data management from inspiring English sources

Exact(7)

All individuals involved in monitoring, data management, or other study aspects were blinded to treatment.

Clinical monitoring, data management, and biometry according to GCP will be conducted by IZKS Mainz.

Clinical monitoring, data management, pharmacovigilance, regulatory affairs and biometry according to GCP were conducted by the IZKS Mainz.

The investigators, study site personnel, and representatives involved in monitoring, data management, any other aspect of the study, including sponsor personnel, were blinded throughout the study.

EB realized the methodology of the study, coordinated the monitoring, data management, statistical analysis, interpretation of the data, and analysis of adverse events, and participated in the writing of the manuscript.

The secretariat supports and assists investigators in the development of protocols and study documents and provides regulatory support, trainings and monitoring, data management and analysis, centralized specimen repository, and laboratory support.

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Similar(53)

Furthermore, we would like to thank the trial nurses and data managers from the Hans Mak Institute (Naarden, The Netherlands) for data monitoring and data management.

This includes having a steering committee that defines inclusion and exclusion criteria, randomization, blinding, placebo control, central monitoring and data management, as well as a data safety and monitory board managed by a preclinical research organization (pCRO).

PMetro is an innovative time/space resolved urban aerosol monitoring and data management system.

The paper therefore emphasises holistic, bottom up assessment of AEC contributions and argues that governments should support such organisations through i) funding for facilitators and ii) funding for impact monitoring and data management.

In my first year at the company, I have learned what is involved in a clinical trial: everything from protocol design, recruitment of investigators and subjects, investigator meetings, the clinical monitoring process, data management, clinical research organizations, adverse event reporting, and so on.

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