Clinical trials are conducted to study the safety and effectiveness of investigational
medicines enabling patients to obtain access to these medicines.
London Clinical Research offers contract consultancy to ensure that clinical research activities are executed according to Good Clinical Practice (GCP) and within expected scope, budget and timelines.
Work closely with colleagues in Biometrics, Clinical Operations, Safety/Pharmacovigilance, Regulatory, Medical Affairs, Molecular Diagnostics, and Translational Research.
Author protocol concepts, synopses, protocols, and amendments
Protocol development and review
Country specific advice
Electronic Clinical record Forms (eCRF) development
Data freeze/unfreeze
Efficacy and safety reviews, SAE reconciliation, query resolution prior to database lock
Update annually clinical data in IB, line extensions
Simple in layman's terms
Reduced size of PIC
Videos more visually appealling
Draft and finalise charters
Write safety patient narratives
London Clinical Research
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