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Staff Resources & Support

SOP 53.011

Sponsor Source Data Requirements and Guidance

SOP 53.010

Monitoring Clinical Research – Preparation and Management of a Monitoring Plan for a Clinical Trial of an Investigational Medicinal Product/Advanced Medicinal Investigation Product/ Medical Device… 

SOP 53.009

Preparation and Maintenance of a Clinical Trial Monitoring File

SOP 53.008

Accompanied and Training Visit Process

SOP 53.007

Unblinded Monitoring Process

SOP 53.006

Monitoring Handover Checklist Process

SOP 53.005

Audit of Research studies and systems supporting research

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