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Staff Resources & Support

SOP 53.006

  • 1 min read

Monitoring Handover Checklist Process

SOP 53.005

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Audit of Research studies and systems supporting research

SOP 53.004

  • 1 min read

Monitoring Clinical Research – Site Monitoring Visit

SOP 53.003

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Temporary Halt or Early Termination of Clinical Trials of Investigational Medicinal Products

SOP 53.002

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The Handling of Poor Quality and Fraud in Clinical Research

SOP 53.001

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Handling urgent safety measures for clinical trials for investigational medicinal products

SOP 52.015

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Phase I First in Human Committee Review Process

SOP 52.014

  • 1 min read

Archiving Essential Documents from Clinical Research – Process for Hosted Research  

SOP 52.013

  • 1 min read

Process for approving studies and trials involving a Genetically Modified Organism (GMO)

SOP 52.009

  • 1 min read

Validation of Project Submissions for R&I Management Approval: NHS