Development of a checklist for the assessment of pharmacovigilance guidelines in Southern Africa: a document review
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Abstract
Introduction: National regulatory systems in Southern Africa reflect various stages of
maturity, and pharmacovigilance (PV) practices are not aligned. In the absence of guidance for
formulating PV guidelines in Southern African Development Community (SADC) countries, this
study aimed to create a checklist that may be used to assess the rigour of PV guidelines in this
region and provide guidance for the National Medicines Regulatory Agency (NMRA) authors.
Methods: A document analysis was performed based on harmonised international guidelines
(n=22) that prescribed methods of PV regulation to identify themes and items to incorporate
into a checklist. The contextualisation of the checklist to the African pharmaceutical
environment was accomplished by referencing peer-reviewed journal articles (n=7). The
checklist was subjected to face and content validation by non-experts and PV experts.
Results: The document review yielded 5 themes, 18 sub-themes, and 73 items structured
into the checklist. Themes encompassed PV systems, definitions, individual case safety
reporting, aggregate reporting, and risk management. Under PV systems, aspects of the
quality management system were outlined, that is, the legal basis for PV, a description of
the marketing authorisation holder's (MAH's) PV system, archiving of data, contracting of PV
tasks, and the duties of the person responsible for the MAH's PV obligations. Definitions of the
key terms and major stakeholders were identified. Reporting of individual case safety reports
(ICSRs) was explicated by considering the criteria for reporting, categories of reportable
information, expedited reporting requirements, reporting timelines, and ICSR reporting
format. Aggregate report submission during the development and post-marketing phases was
addressed. Risk management encompassed signal detection, re-evaluation of the benefit-risk
ratio, the safety decision-making process, risk management planning, risk minimisation and
safety communication.
Conclusion: The developed checklist can contribute towards assisting SADC NMRAs to
formulate national PV guidelines that reflect current international practice, with local context
incorporated.
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Citation
Nokuthula L. Makhene, Hanlie Steyn, Martine Vorster, Martie S. Lubbe and Johanita R. Burger. 2023. Development of a checklist for the assessment of pharmacovigilance guidelines in Southern Africa: a document review.https://doi.org/10.1177/20420986221143272
