ISSN: 2167-0870
Department of Adult Cystic Fibrosis, Royal Brompton Hospital, London, UK
Dr. Rebecca Dobra is currently working in Department of Adult Cystic Fibrosis, Royal Brompton Hospital, London, UK. She has published numerous research papers and articles in reputed journals and has various other achievements in the related studies. She has extended her valuable service towards the scientific community with her extensive research work.
Research Article
Strengthening Clinical Trial Pharmacovigilance: Simple Interventions Improve Communication Over Serious Adverse Events
Author(s): Rebecca Dobra*, Katherine Huband, Jessie Matthews, Sandra Scott, Nicholas Simmonds and Jane Davies
With over 100 drugs in the development pipeline, this is an exciting time for drug development in Cystic Fibrosis (CF). However, the increased number of trial participants brings challenges. Unscheduled admissions of clinical trial participants are defined as Serious Adverse Events (SAEs). Good Clinical Practice (GCP) guidelines mandate prompt reporting of SAEs to optimise pharmacovigilance and protect patient safety. As our trial cohort grew, so did our trial team, with junior roles becoming trial or clinical specific. Consequently, we encountered delayed awareness by the trials team of unplanned admissions. We conducted a quality improvement (QI) project to empower clinical teams to act as a safety net to alert trial teams to admissions of trials patients to improve patient safety and optimise pharmacovigilance through timely SAE reporting on clinical trials.
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DOI:
10.35248/2167-0870.20.S7.001