2019
DOI: 10.3390/ijerph16111972
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Critical Success Factors of a Drug Traceability System for Creating Value in a Pharmaceutical Supply Chain (PSC)

Abstract: The general objective of this study was to identify and prioritize the critical success factors required for the adoption of a system to create value for pharmaceutical supply chain stakeholders, and the pharmaceutical supply network as a whole, by using a multi-perspective framework that combines elements of the technology–organization–environment (TOE) contexts for enterprises. The methodology is based on a literature review and expert interviews following the analytic hierarchy process (AHP). This paper ide… Show more

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Cited by 32 publications
(42 citation statements)
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“…We adopted a 5-tier model of pharmaceutical supply chains consisting of primary manufacturer of active pharmaceutical ingredient (API) (Tier 1), secondary manufacturer of finished pharmaceutical product (FPP) (Tier 2), main distributor (Tier 3), local distributor (Tier 4), and demand point (Tier 5). 27 The scoping review methodology was adopted to enable comprehensive data collection, considering that some of the information sought on these players and processes in the supply chain may not be available as peer-reviewed literature.…”
Section: Methodsmentioning
confidence: 99%
“…We adopted a 5-tier model of pharmaceutical supply chains consisting of primary manufacturer of active pharmaceutical ingredient (API) (Tier 1), secondary manufacturer of finished pharmaceutical product (FPP) (Tier 2), main distributor (Tier 3), local distributor (Tier 4), and demand point (Tier 5). 27 The scoping review methodology was adopted to enable comprehensive data collection, considering that some of the information sought on these players and processes in the supply chain may not be available as peer-reviewed literature.…”
Section: Methodsmentioning
confidence: 99%
“…In addition, waste management also requires effective segregation of waste, which is key to reducing the volume of waste that needs attention and ensuring that each treatment process only receives compatible waste [ 55 ]. The introduction of a digital track and trace system would provide timely information to support the production and distribution of medicines in order to optimise medicine production and reduce overproduction, which leads to the generation of waste [ 55 , 56 , 57 ].…”
Section: Resultsmentioning
confidence: 99%
“…To operationalize the assessment of the recommendation, we used the medicine supply chain “framework” by Silva et al, 2019. We adapted it to describe nodes at which quality assurance mechanisms would be required [ 39 ]. Eight mechanisms covering four nodes and the presence of a National Medicines Regulatory Authority were framed as criteria for assessing the NAPs.…”
Section: Methodsmentioning
confidence: 99%