Research map: An evaluation of the use of the Universal Benefit–Risk Assessment Framework by the Zambia Medicines Regulatory Authority for documenting and communicating benefit–risk decisions.
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Papers in this map
Structured Frameworks to Increase the Transparency of the Assessment of Benefits and Risks of Medicines: Current Status and Possible Future Directions
· Francesco Pignatti · 2015 · 48 citations · Cited by this paper
In silico prediction of Ames mutagenicity for organosilicon compounds: Exploring and enhancing chemical space boundaries
· 2026 · Related
A Universal Framework for the Benefit-Risk Assessment of Medicines: Is This the Way Forward?
· Stuart Robert Walker · 2014 · 39 citations · Cited by this paper
Standardization and Assessment of Acute Dermal Toxicity of an Ayurvedic Medicine Brihat Somraji Taila in Sprague-Dawley rats
· 2026 · Related
Real‐world evidence to support regulatory decision making: New or expanded medical product indications
· Jessica Myers Franklin · 2021 · 36 citations · Cited by this paper
Evaluating dosing guidelines for Ginkgo biloba: An evidence-based approach to standardisation
· 2026 · Related
Advancing structured decision‐making in drug regulation at the FDA and EMA
· Aris Angelis · 2020 · 34 citations · Cited by this paper
Dietary intake and health risk characterization of cadmium, lead, and mercury in milkfish (Chanos chanos) and tilapia (Oreochromis spp.) from aquaculture farms surrounding Manila bay, Philippines
· 2026 · Related
WHO collaborative registration procedure using stringent regulatory authorities’ medicine evaluation: reliance in action?
· Alexandra Vaz · 2022 · 32 citations · Cited by this paper
Polycyclic aromatic hydrocarbon (PAH) contamination in clinical nutrition: Levels and associated health risks in enteral nutrition formulas
· 2026 · Related
Multi-Criteria Decision Analysis for Benefit-Risk Analysis by National Regulatory Authorities
· Orin T. Chisholm · 2022 · 30 citations · Cited by this paper
Automated extraction of toxicological mechanism of action from PubMed literature using Large Language Models
· 2026 · Related
Benefit-Risk Assessments at the US Food and Drug Administration
· Robert M. Califf · 2017 · 29 citations · Cited by this paper
Derivation of an occupational exposure limit (OEL) for a potent bispecific protein—Blinatumomab (BLINCYTO®)
· 2026 · Related
The Benefit-Risk Assessment of Medicines: Experience of a Consortium of Medium-Sized Regulatory Authorities
· Neil McAuslane · 2017 · 23 citations · Cited by this paper
Microplastics in intravenous fluids: Occurrence, characterization, and risk indicators
· 2026 · Related
Can Standardisation of the Public Assessment Report Improve Benefit-Risk Communication?
· Andrea Keyter · 2020 · 11 citations · Cited by this paper
Food enzyme safety: an extensive lineage of safe Aspergillus niger production strains
· 2026 · Related
Pharmacovigilance Principles: The Building Blocks of Benefit-Risk Assessments
· Rosa Piccirillo · 2022 · 4 citations · Cited by this paper
40-week repeat-dose toxicity, toxicokinetics, and immunogenicity of efsubaglutide alfa following subcutaneous administration in cynomolgus monkeys
· 2026 · Related
Health Technology Agency insights: informing modification of a qualitative benefit risk framework for Health Technology Reassessment of prescription medications
· Mary Alison Maloney · 2019 · 3 citations · Cited by this paper
Analysis Considerations for Real-World Evidence and Clinical Trials Related to Safety
· Richard C. Zink · 2021 · 2 citations · Cited by this paper
The value of a structured, systematic approach to benefit-risk assessment of medicines: A South African regulator case study
· Lorraine Danks · 2025 · 2 citations · Cited by this paper
Mapping the cancer research landscape across Zambia: evidence to support national cancer control planning
· Susan Msadabwe · 2025 · 1 citation · Cited by this paper
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