Staff & Recruitment

Clinical Portal Access for External Users in GCRF

PV Office Processing for Clinical Investigations of Non CE/UKCA Marked medical Devices

Summary of Product Characteristics (SmPC) & Investigator’s Brochure Checks

PV Office – Handling Drug Alerts

PV Office – Processing for Non-CTIMP Studies

Completion Guidelines: Generic Non-CTIMP Serious Adverse Event Form

PV Office – Creation and submission of Development Safety Update Reports

PV Office Processing for Clinical Trials of Investigational Medicinal Products

PV Office – Pharmacovigilance File

PV Office – Submitting SUSAR reports to MHRA via ICSR