Skip to content
Home > Staff & Recruitment > Staff Resources & Support > Page 95

Staff Resources & Support

SOP 55.017

Sponsor Quality Control of SAEs Processed by the Pharmacovigilance Office

SOP 55.015

Sponsor Pharmacovigilance Data

SOP 55.007

Safety Reporting In Clinical Trials Of Non CE/UKCA Marked Medical Devices Or CE/UKCA Marked Devices Used Outside Of Their Intended Purpose (Sponsored And Hosted Clinical… 

SOP 55.006

  • 1 min read

Selection and Periodic Review of IBs and SmPCs in CTIMPs for Clinical Management

SOP 55.005

  • 1 min read

Management of Reference Safety Information for Clinical Trials of IMPs (including ATMPS)

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