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Staff & Recruitment

SOP 55.004

Safety RepSafety Reporting Requirements for Research Other Than Clinical Trials of Investigational Medicinal Products and non CE Marked Medical Devices

SOP 55.002

Preparation and Submission of the Development Safety Update Report

SOP 55.001

Pharmacovigilance in Clinical Trials of Investigational Medicinal Products (Glasgow Clinical Trials Unit)

SOP 53.013

Monitoring Clinical Research – For Cause Monitoring Visit

SOP 53.012

Monitoring Clinical Research – Site Close Out Monitoring visit

SOP 53.011

Sponsor Source Data Requirements and Guidance

SOP 53.010

Monitoring Clinical Research – Preparation and Management of a Monitoring Plan

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