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DTSTART:19700329T010000
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DTSTART:19701025T020000
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SUMMARY:Good Clinical Practice (GCP) for Labs
DTSTART;TZID=Europe/London:20261014T123000
DTEND;TZID=Europe/London:20261014T163000
DTSTAMP:20260626T203401Z
UID:cec75c0f-bc4e-f111-bec7-7c1e52046848
CREATED:20260513T110828Z
DESCRIPTION:Laboratories handling samples derived from Clinical Trials of 
 Investigational Medicinal Products (CTIMPs) are legally obliged to adhere 
 to Good Clinical Practice (GCP). But what does this mean in practice? \nTh
 is course will provide a brief overview of CTIMP design and delivery\, the
 n guide you through the principles of GCP and what this means from the per
 spective of the laboratory. Key areas covered include:\n\n>Requirements of
  a Quality Management System\n>Roles and responsibilities\n>Participant co
 nsent \n>Ensuring data integrity\n>Managing errors\, deviations and incide
 nts\n>Archiving\n>MHRA inspections\n\nEmail rgea.training@admin.ox.ac.uk t
 o book this session date.
LAST-MODIFIED:20260513T145028Z
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