EVALUASI PENYIMPANAN OBAT DAN ALAT KESEHATAN DI APOTEK REJEKI LESTARI
DOI:
https://doi.org/10.59060/4ck4zb88Abstract
The storage of medicines and medical devices is an important component in the implementation of pharmaceutical services, as it affects the quality, stability, safety, and therapeutic effectiveness of these products. Non-standard storage management may lead to active ingredient degradation, reduced quality of medical devices, and potential risks to patient safety. The implementation of an appropriate and regulation-based storage system plays a vital role in ensuring the quality of pharmaceutical services in healthcare facilities. The purpose of this study is to assess the compliance of drug and medical device storage at Apotek Rejeki Lestari with Technical Guidelines for the Implementation of Pharmaceutical Services issued by the Ministry of Health of the Republic of Indonesia at 2019. This study employed a descriptive observational method through direct observation. The measurement instrument used was a checklist consisting of 25 statements. Data collection was conducted in May 2025. The data were analyzed descriptively by calculating the percentage of storage compliance with the standards. The results showed that the overall storage aspects complied with the standards, with 21 indicators having been fulfilled. There were 4 indicators that did not meet the storage standards. The noncompliant aspects included the absence of an air conditioner to maintain room temperature and the lack of storage cabinets for High-Alert Medications (HAM), as well as for expired and damaged drugs. In conclusion, the storage system at Apotek Rejeki Lestari is very good, with a compliance rate of 84%; although improvements are needed in the aspect of high-risk medication.
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