Results 61 to 70 of about 1,185 (135)

Quality Infrastructure for Resilient Pharmaceutical Manufacturing in Ethiopia: A Comparative Archival Review

Journal of Critical Infrastructure Policy, Volume 7, Issue 1, Spring/Summer 2026.
ABSTRACT The National Quality Infrastructure (NQI) in a given country provides the essential framework for quality assurance integrating standardization, metrology, accreditation, and conformity assessment to create the technical backbone for industry and trade. Hence, building a resilient NQI is fundamental to securing medicine quality, enabling local
Addisu Afrassa Tegegne, Mesfin Demissie Woldecherkos, Habtewold Deti Waktola, Sultan Suleman   +3 more
wiley   +1 more source

Blockchain and Quantum Technologies for Securing the Global Nuclear Supply Chain: Synergies, Applications, Technical Challenges and Opportunities

Journal of Critical Infrastructure Policy, Volume 7, Issue 1, Spring/Summer 2026.
ABSTRACT The infiltration of counterfeit, fraudulent, and suspect items into civil nuclear supply chains, notably within power generation and medical isotope production, poses severe safety and security threats. The ever‐increasing growth in nuclear installations (70 power plants are under construction and another 100 are in the planning stage) and the
Hafiz Ahmed
wiley   +1 more source

Use of Blockchain Technology in the Pharmaceutical Industry to Track Medicines in Zambia

IET Blockchain, Volume 6, Issue 1, January/December 2026.
The main aim of the project was to design and implement a system that uses blockchain technology to solve the problem of counterfeit or outdated drugs in the Zambian market by providing a decentralised and reliable way of tracking medicines throughout the distribution chain.
Derrick Ntalasha, Michael Sinkolongo
wiley   +1 more source

Laboratory evaluation of twelve portable devices for medicine quality screening.

PLoS Neglected Tropical Diseases, 2021
BackgroundPost-market surveillance is a key regulatory function to prevent substandard and falsified (SF) medicines from being consumed by patients. Field deployable technologies offer the potential for rapid objective screening for SF medicines.Methods ...
Stephen C Zambrzycki, Celine Caillet, Serena Vickers, Marcos Bouza, David V Donndelinger, Laura C Geben, Matthew C Bernier, Paul N Newton, Facundo M Fernández   +8 more
doaj   +1 more source

Regulating Artificial Intelligence as a Medical Device (AIaMD) in Africa: The Role of Regulatory Sandboxes in Bridging Current GAPS

Advances in Public Health, Volume 2026, Issue 1, 2026.
Africa’s medical device industry is undergoing exponential growth. It was valued at about $4.26 billion (USD) in 2025, with projections that it will grow to $7.14 billion by 2032, significantly outpacing global averages. The increased technological advancements in medical devices, driven by artificial intelligence (AI) and the continent’s desire to ...
Kalule Grancia Mugalula, Haipeng Liu
wiley   +1 more source

Usefulness of combined screening methods for rapid detection of falsified and/or substandard medicines in the absence of a confirmatory method

Malaria Journal, 2019
Background The influx of substandard and falsified medicines is a global public health challenge and its rapid detection is a key solution to the menace. This study used three screening methods and one confirmatory method for the quality assessment of 25
Kwabena Frimpong-Manso Opuni, Henry Nettey, Marvin Adjei Larbi, Salome Naa Amerley Amartey, Gifty Nti, Abraham Dzidonu, Patrick Owusu-Danso, Nicholas Amoah Owusu, Alexander Kwadwo Nyarko   +8 more
doaj   +1 more source

Gaps in Veterinary Pharmaceuticals and Pesticide Regulation: GMP Compliance, Postmarket Surveillance, and Institutional Reforms

Veterinary Medicine International, Volume 2026, Issue 1, 2026.
Background In Ethiopia, veterinary pharmaceuticals and agricultural pesticides are vital to maintaining agricultural productivity and food security, yet their quality and safety regulation face significant challenges. Objectives This study aimed to assess the regulatory framework, institutional capacity, and routine quality assurance practices related ...
Yesuneh Tefera Mekasha, Hassen Kebede Hassen, Mikael Abraham, Mulukan Akalu Shiferaw, Dejene Asaye Mengistu, Zerihun Mesfin Girma, Eshet Emiru Nigussie, Yildiz Ozalp, Lipi Buch   +8 more
wiley   +1 more source

Designing Physical Unclonable Functions From Optically Active Materials

Advanced Materials, Volume 37, Issue 49, December 10, 2025.
Assigning unforgeable “fingerprints” to manufactured goods is a key strategy to fight global counterfeiting. Optical physical unclonable functions (PUFs) are chemically generated random patterns of optically active materials serving as unique authenticators.
Maxime Klausen, Junfang Zhang, Molly M. Stevens   +2 more
wiley   +1 more source

Development of an agent-based model to assess the impact of substandard and falsified anti-malarials: Uganda case study

Malaria Journal, 2019
Background Global efforts to address the burden of malaria have stagnated in recent years with malaria cases beginning to rise. Substandard and falsified anti-malarial treatments contribute to this stagnation.
Sachiko Ozawa, Daniel R. Evans, Colleen R. Higgins, Sarah K. Laing, Phyllis Awor   +4 more
doaj   +1 more source

Evaluation of community pharmacists’ readiness to implement the Falsified Medicines Directive (Directive 2011/62/EC): an English cross-sectional survey with geospatial analysis

BMJ Open, 2020
Objectives To evaluate the readiness to implement the Falsified Medicines Directive (FMD) by community pharmacies in England. Eight secondary objectives were assessed.Setting Community/retail pharmacies.Participants We invited pharmacists from 501 ...
Ravina Barrett
doaj   +1 more source