Risk-proportionate clinical trial monitoring: an example approach from a non-commercial trials unit

Background Some level of monitoring is usually required during a clinical trial to protect the rights and safety of trial participants and to safeguard the quality and reliability of trial results. Although there is increasing support for the use of risk-proportionate approaches to achieve these ai...

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Bibliographic Details
Main Authors: Smith, Catrin Tudur, Williamson, Paula, Jones, Ashley, Smyth, Alan R., Hewer, Simon Langton, Gamble, Carrol
Format: Article
Published: BioMed Central 2014
Subjects:
Online Access:https://eprints.nottingham.ac.uk/31675/