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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

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

SOP 52.007

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Authorisations for NHS Resource use in R&I Systems Submissions

SOP 52.005

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

SOP 52.004

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R&I Contract Development and Review

SOP 52.003

  • 1 min read

R&I Local Review of Modifications