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SOP 53.004

Monitoring Clinical Research – Site Monitoring Visit

SOP 53.003

Temporary halt or early termination of clinical trials of investigational medicinal products

SOP 53.002

The Handling of Poor Quality and Fraud in Clinical Research

SOP 53.001

Handling urgent safety measures for clinical trials for investigational medicinal products

SOP 52.015

Phase I First in Human Committee Review Process

SOP 52.014

Archiving Essential Documents from Clinical Research – Process for Hosted Research

SOP 52.013

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

SOP 52.009

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

SOP 52.007

Authorisations for NHS resource use in R&D submissions

SOP 52.005

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