Jul 2026· Universal Library of Innovative Research and Studies· Vol 3, pp. 20-25· 0 citations· 9 references
TL;DR
The analysis demonstrates that the highest level of sustainability is achieved in models where test automation is embedded within a formalized quality-management framework and used as a mechanism for preventing risks associated with digital change.
Abstract
This article presents an analytical synthesis of approaches to de-risking the digital transformation of healthcare organizations based on SAP S/4HANA through automated quality assurance. The study is conducted as a systematic analysis of peer-reviewed scientific sources and focuses on interpreting the quantitative effects of test automation in terms of change controllability rather than solely development efficiency. Particular attention is paid to measurable indicators of release speed, test coverage, system recovery resilience, and behavioral predictability under frequent updates, as well as to their role in forming managed quality control loops. It is shown that the key factor of transformation sustainability is the extent to which critical quality-assurance risk areas—related to test authoring, maintenance, execution, and result formalization—are addressed, rather than the mere presence of automated test scripts. It is established that, in the healthcare context, the applicability of automation is determined by its integration into the computer system validation lifecycle and change-control processes that ensure requirements traceability and test reproducibility. The analysis demonstrates that the highest level of sustainability is achieved in models where test automation is embedded within a formalized quality-management framework and used as a mechanism for preventing risks associated with digital change. The article is of interest to researchers in digital health, enterprise information system architects, quality and validation specialists, and practitioners involved in transforming SAP landscapes in regulated environments.
A macroprocess model is proposed that organizes, operationalizes, and monitors the requirements of the WHO’s Quality Practices in Basic Biomedical Research (QPBR) Manual, adapting it to the practical/operational reality of laboratories.
S. L. C. Fernandez, R. A. de Souza, H. S. da Hora et al.· JOURNAL OF BIOENGINEERING, T...· 0 citations
Background: Digital transformation is reshaping healthcare through the
integration of electronic health records, telemedicine, artificial intelligence,
automation, connected devices, data analytics, and interoperable digital
platforms. However, the extent to which these technologies translate into
measurable improvemen...
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Oscar A. Betancur Salazar, Alejandra Cadavid Marín, Nayid Triana Guzmán· 2026 IEEE Colombian Conferen...· 0 citations
This work proposes nine operational measures - covering transparency-oriented risk and change control, traceability, subgroup and independent validation, usability-based explainability, calibrated clinical evaluation, structured labeling, version-controlled updates, and regulated end-of-life data handling - to support...
E. Bianchini, L. Billeci, Noemi Conditi et al.· Expert Review of Medical Dev...· 0 citations
Introduction. The quality of public regulation of medicines circulation depends on a management control system that ensures the timeliness, quality, and transparency of expert processes. Traditional reporting mainly records deviations after they have occurred, which creates a need for a model that enables early risk id...
Azamat Seisenov, S. Mamyrbekova· Farmaciâ Kazahstana· 0 citations
Understanding the interplay among the SDGs, the digitalization of health systems, and shifting patient expectations is vital for designing equitable, sustainable, and high-quality care frameworks.
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