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Staff Resources & Support

SOP 53.004

  • 1 min read

Monitoring Clinical Research – Site Monitoring Visit

SOP 53.003

  • 1 min read

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

SOP 53.002

  • 1 min read

The Handling of Poor Quality and Fraud in Clinical Research

SOP 53.001

  • 1 min read

Handling urgent safety measures for clinical trials for investigational medicinal products

SOP 52.015

  • 1 min read

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

SOP 52.007

  • 1 min read

Authorisations for NHS Resource use in R&I Systems Submissions

SOP 52.005

  • 1 min read

Review of Research Passport and issuing of Honorary Research Contracts/Letters of Access