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Staff Resources & Support

SOP 56.004

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Project Management Trial Site Close-Out

SOP 56.003

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Project Management: Managing an Active Trial

SOP 56.002

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Project Management Trial Set-up

SOP 56.001

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Site Set up – Green for Go Process

SOP 55.016

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Sponsor IB Assessment

SOP 55.017

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Sponsor Quality Control of SAEs Processed by the Pharmacovigilance Office

SOP 55.015

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Sponsor Pharmacovigilance Data

SOP 55.007

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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… 

Continue reading >SOP 55.007

SOP 55.006

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

SOP 55.005

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