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Staff Resources & Support

SOP 56.004

Project Management Trial Site Close-Out

SOP 56.003

Project Management: Managing an Active Trial

SOP 56.002

Project Management Trial Set-up

SOP 56.001

Site Set up – Green for Go Process

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)