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Max SchurerMy Pharmacovigilance Journey as an Industrial Engineering PhD Student After studying molecular biology and biotechnology Max undertook his pharmacovigilance-focusesd PhD at the Deparment of Industrial Engineering, Stellenbosch University, South Africa. Max's research focused on the interoperability of spontaneous reporting systems (SRSs) in pharmacovigilance, specifically guiding SRSs towards interoperability through the introduction of a capability maturity model. |
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Ernest Dela DzidzornuMy Journey to Becoming a QPPV in Ghana Ernest works in the Department of Pharmacovigilance and Regulatory Affairs as a Qualified Person for Pharmacovigilance (QPPV) at Salom Pharmacy Limited, Kumasi, Ghana. In this article, Ernest describes his journey to becoming a QPPV, his roles and responsibilties, and provides his thoughts on the current challenges facing pharmacovigilance in Ghana. One of Ernest's many interests is finding ways to boost the spontaneous ADR reporting rates in Ghana. |
Biancé Huysamen
My Pharmacovigilance Journey: Biancé undertook her pharmacovigialnce-focused Masters degree at the Department of Industrial Engineering, Stellenbosch University, South Africa. Biancé's research examined how niche environmental factors affect drug safety monitoring systems and led to the development of a conceptual framework for a 'Niche PV System' that can take the unique needs of these factors into account. |
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Walter-Rodney NagumoUndertaking a PhD in Pharmacovigilance After completing a bachelor's degree in biology and then a Masters of Science in Clinical Trials at the University of Ghana, Rodney began his PhD at the School of Health and Related Research (ScHARR), University of Sheffiled, UK. Rodney's research aimed to understand pharmacovigilance and ADR reporting practices among healthcare professionals in Ghana. Rodney has also written on social media as a pharmacovigilance tool in Africa. |
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Cheryl PaceMy Career as a Pharmacovigilance Pharmacist |
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Elizabeth AllenMy Journey to a Pharmacovigilance PhD Liz is Head of Clinical Research at the Collaborating Centre for Optimising Antimalarial Therapy (CCOAT), University of Cape Town. She began her PhD in pharmacovigilance after working as a community pharmacist, and in clinical trials. Liz has a research interest in the assessment of drug safety in clinical trials and also coordinates globalpharmacovigilance.org. |
Paul Cross My Pharmacovigilance PhD Journey Paul is the GCP Quality Assurance Manager at Guy's and St Thomas' NHS Foundation Trust, London, UK. He first considered a PhD in Pharmacovigilance whilst completeing his MSc in Clinical Research. Paul has a research interest in patient and public involvement and engagement (PPIE) and pharmacovigilance in clinical trials. |
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