Securing the Chain of Custody and Integrity of Data in a Global North–South Partnership to Monitor the Quality of Essential Medicines

Substandard and falsified (SF) pharmaceuticals account for an estimated 10% of the pharmaceutical supply chain in low-and middle-income countries (LMICs), where a lack of regulatory and laboratory resources limits the ability to conduct effective post-market surveillance and allows SF products to pe...

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Bibliographic Details
Main Authors: Ashenef, A. (Author), Hayes, K. (Author), Johann, T. (Author), Kochalko, D. (Author), Lieberman, M. (Author), Meyers, N. (Author), Sweet, C. (Author)
Format: Article
Language:English
Published: Partners in Digital Health 2022
Subjects:
Online Access:View Fulltext in Publisher
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008 220706s2022 CNT 000 0 und d
020 |a 25738240 (ISSN) 
245 1 0 |a Securing the Chain of Custody and Integrity of Data in a Global North–South Partnership to Monitor the Quality of Essential Medicines 
260 0 |b Partners in Digital Health  |c 2022 
856 |z View Fulltext in Publisher  |u https://doi.org/10.30953/bhty.v5.230 
520 3 |a Substandard and falsified (SF) pharmaceuticals account for an estimated 10% of the pharmaceutical supply chain in low-and middle-income countries (LMICs), where a lack of regulatory and laboratory resources limits the ability to conduct effective post-market surveillance and allows SF products to penetrate the supply chain. The Distributed Pharmaceutical Analysis Laboratory (DPAL) was established in 2014 to expand testing of pharmaceutical dosage forms sourced from LMICs; DPAL is an alliance of academic institutions throughout the United States and abroad that provides high-quality, validated chemical analysis of pharmaceutical dosage forms sourced from partners in LMICs. Results from analysis are reported to relevant regulatory agencies and are used to inform purchasing decisions made by in-country stakeholders. As the DPAL program has expanded to testing more than 1,000 pharmaceutical dosage forms annually, challenges have surfaced regarding data management and sample tracking. Here, we describe a pilot project between DPAL and ARTiFACTs that applies the blockchain to organize and manage key data generated during the DPAL workflow, including a sample’s progress through the workflow, its physical location, provenance of metadata, and lab reputability. Recording time and date stamps with these data will create a permanent and verifiable chain of custody for samples. This secure, distributed ledger will be linked to an easy-to-use dashboard, allow-ing stakeholders to view results and experimental details for each sample in real time and verify the integrity of DPAL analysis data. Introducing this blockchain-based system as a pilot will allow us to test the technology with real users analyzing real samples. Feedback from users will be recorded and necessary adjustments will be made to the system before the implementation of blockchain across all DPAL sites. Anticipated benefits of implementing the blockchain technology for managing DPAL data include efficient management for routing work, increasing throughput, creating a chain of custody for samples and their data in alignment with the distributed nature of DPAL, and using the analysis results to detect patterns of quality within and across brands of products and develop enhanced sampling techniques and best practices. © 2022, Partners in Digital Health. All rights reserved. 
650 0 4 |a analytical chemistry 
650 0 4 |a blockchain 
650 0 4 |a ledger 
650 0 4 |a pharmaceutical 
650 0 4 |a quality of medicine 
650 0 4 |a supply chain 
700 1 |a Ashenef, A.  |e author 
700 1 |a Hayes, K.  |e author 
700 1 |a Johann, T.  |e author 
700 1 |a Kochalko, D.  |e author 
700 1 |a Lieberman, M.  |e author 
700 1 |a Meyers, N.  |e author 
700 1 |a Sweet, C.  |e author 
773 |t Blockchain in Healthcare Today