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Journal articles on the topic 'Pharmaceutical Storage Guidelines'

Author: Grafiati
Published: 7 June 2025
Last updated: 2 August 2025

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1

Endiyonarsi, Endiyonarsi, Nilawati Uly, Achmad R. Muttaqien Al-Maidin, and Zamli Zamli. "Analysis of Drug Management in the Pharmaceutical Installation of the South Sorong District Health Office." Healthy Tadulako Journal (Jurnal Kesehatan Tadulako) 11, no. 1 (2025): 70–80. https://doi.org/10.22487/htj.v11i1.1515.

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Background: The management of pharmaceutical supplies involves a series of coordinated activities related to the planning, procurement, storage, distribution, and disposal of drugs, aimed at ensuring the availability and appropriate use of medications. Objectives: This study aims to describe the implementation pattern of pharmaceutical supply management, focusing on the processes of planning, procurement, and storage at the Pharmacy Installation of the South Sorong Regency Health Office. Methods: A qualitative research design was used, employing in-depth interviews with key informants to gathe
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S., D. Mankar Shruti Varade Vaibhav Varghude Sagar Vendait* Atharv Vikhe Mayur Wagh. "A Review on Good Warehousing Practices." International Journal of Pharmaceutical Sciences 3, no. 4 (2025): 2287–94. https://doi.org/10.5281/zenodo.15240493.

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In the pharmaceutical industry, warehousing is an integral part of the supply chain, ensuring the safe storage, handling, and distribution of medicines and related products. Given the sensitive nature of pharmaceutical goods, warehouses must comply with stringent regulatory standards, including Good Manufacturing Practice (GMP) and Good Distribution Practice (GDP). This review provides an overview of the critical need for pharmaceutical warehouses, the layout considerations that support operational efficiency, and the guidelines that govern their operation. Furthermore, it highlights the benef
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Malik, Anuj, Gourab Gochhayat, Md Shamshir Alam, et al. "Quality by Design: A new practice for production of pharmaceutical products." Journal of Drug Delivery and Therapeutics 9, no. 1-s (2019): 416–24. http://dx.doi.org/10.22270/jddt.v9i1-s.2370.

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This is the advanced approach for development of pharmaceutical product with full range and specified limits of variables during procurements, storage and manufacturing process with a qualification, at desired level of quality within the limits of low and higher values of variables to ensures the Pharmaceutical product Quality by design (QbD) of manufacturing a finished product. The Quality by Design is depicted and a portion of its components recognized and process parameters with quality characteristics are identified for every unit activity. Advantages, openings and steps engaged with Quali
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Dini Nurdwiyanti, Puspa, A. Mumtihanah Mursyid, and Vina Purnamasari. "Gambaran Penyimpanan Obat di Rumah Sakit Umum Daerah Hajjah Andi Depu Kabupaten Polewali Mandar." Makassar Pharmaceutical Science Journal (MPSJ) 1, no. 4 (2024): 329–36. https://doi.org/10.33096/mpsj.v1i4.107.

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Drug storage is an important stage in the drug management because proper drug storage can maintain drug quality, prevent irresponsible drug use, prevent theft and facilitate drug search and control in hospitals. The impact of the storage process that is not in accordance with pharmaceutical requirements is that the availability of drugs is not maintained and there is the potential for irresponsible drug use resulting in losses for the Hospital. The purpose of this study was to find out an overview of drug storage at the Hajjah Andi Depu General Hospital, Polewali Mandar Regency. This study use
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Syahyeri, Afrizal. "The Evaluation Of Drug Storage at The Pharmacy Warehouse Gamping 1 Health Center, Sleman Regency." Journal of health research and technology 3, no. 2 (2025): 130–44. https://doi.org/10.58439/jhrt.v3i2.276.

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Introduction: Pharmaceutical services at community health center include 2 (two) activities include the management of pharmaceutical preparations and consumable medical materials and clinical pharmacy service activities. One of the pharmaceutical preparation management activities is drug storage. Drug storage is one way to guarantee the quality of drugs so that they are safe. Objective: To evaluate the drug storage at the Gamping 1 Health Center, Sleman Regency. Methods: This research design is a descriptive non-experimental study using a cross sectional approach. Using a checklist sheet guide
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Qurratul Ain Leghari, Noshad, Neha Tehreem Anwar, Yumna Syed, Ali Asgher Shuja, and Mehtab Ali. "Ensuring Pharmaceutical Quality: The Role of Stability Studies and Regulatory Guidelines: A Review." Indus Journal of Bioscience Research 3, no. 3 (2025): 112–22. https://doi.org/10.70749/ijbr.v3i3.942.

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Objective: To ensure the quality of pharmaceutical products, stability studies are mandated. These studies adhere to guidelines established by organizations such as the International Conference on Harmonization (ICH) (e.g., ICH Q1AR2) and the World Health Organization (WHO). They evaluate how well the products maintain their physical, chemical, microbiological, and other essential properties under defined conditions. Methodology: This section dives into the world of stability testing for drugs and pharmaceuticals. We'll explore the different types of assessments used to monitor a product's qua
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Impa, Elson, Yunita Nita, and Yuni Priyandani. "Profile of the management of pharmaceutical products and medical consumables at primary healthcare centres in North Toraja district." Pharmacy Education 23, no. 4 (2023): 331–35. http://dx.doi.org/10.46542/pe.2023.234.331335.

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Background: The management of pharmaceutical products and medical consumables in primary healthcare centres (PHCs)should be efficient, effective, and rational. Management is one of the competencies of pharmacists. Objective: This study aimed to describe the management profile of pharmaceutical products and medical consumables at primary healthcare centres in the North Toraja district. Method: This cross-sectional study used a questionnaire to collect data. The indicator for managing pharmaceutical products and medical consumables was based on technical guidelines for pharmaceutical service sta
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Taswin, Muhammad, Sarmadi Sarmadi, and Tedi Tedi. "GAMBARAN PENYIMPANAN SEDIAAN FARMASI PADA PEDAGANG BESAR FARMASI DI KOTA PALEMBANG." JKPharm Jurnal Kesehatan Farmasi 4, no. 2 (2022): 1–8. http://dx.doi.org/10.36086/jpharm.v4i2.1238.

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ABSTRAK
 
 Latar Belakang: Kesalahan dalam proses penyimpanan masih menjadi penyebab terbesar kerusakan pada sediaan farmasi yang dapat berdampak pada keselamatan pasien. Sebelum sediaan farmasi sampai ke tangan pasien diperlukan instansi kesehatan yang terlibat dalam kegiatan pendistribusian, yaitu Pedagang Besar Farmasi (PBF). Untuk menjamin keamanan, khasiat dan mutu sediaan farmasi maka PBF perlu menerapkan operasional penyimpanan yang termasuk dalam salah satu aspek penting pada Pedoman Cara Distribusi Obat yang Baik (CDOB).
 Metode: Penelitian ini merupakan penelitian non
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Lalwani, Parag Mangilal* R. B. Darade. "Overview of regulatory guidelines for stability study of pharmaceuticals." International Journal in Pharmaceutical Sciences 2, no. 5 (2024): 141–46. https://doi.org/10.5281/zenodo.11109892.

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The safety, efficacy and quality of a pharmaceutical product plays a crucial role in product development, stability study ensures the following about the product.  Shelf life of a product is consider for its acceptance and approval. These stability studies are conducted by following guidelines issued by international regulatory agencies such as ICH, WHO etc. These guidelines provide a plan to conduct the stability study, various methods are involved in performing stability studies. The environment plays an important role in quality of a product, the stability studies helps to retain produ
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Hidayati, Nuning Vita, Laurence Asia, Stephanie Lebarillier, et al. "Environmental Sample Stability for Pharmaceutical Compound Analysis: Handling and Preservation Recommendations." Journal of Analytical Methods in Chemistry 2023 (October 19, 2023): 1–10. http://dx.doi.org/10.1155/2023/5526429.

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Efficient and resilient techniques for handling samples are essential for detecting pharmaceutical compounds in the environment. This study explores a method for preserving water samples during transport before quantitative analysis. The study investigates the stability of 17α-ethynylestradiol (EE2), acetaminophen (ACM), oxytetracycline (OTC), sulfamethoxazole (SMX), and trimethoprim (TMP) after preconcentration within solid-phase extraction (SPE) cartridges. Through various experiments involving different holding times and storage temperatures, it was determined that four pharmaceutical compo
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Krychkovska, Aelita, Nataliya Zayarnyuk, Oksana Lopatynska, Roksolana Konechna, Nataliia Polish, and Volodymyr Novikov. "LEARNING GOOD PHARMACEUTICAL PRACTICES AS A COMPONENT OF PROFESSIONAL TRAINING OF PHARMACY SPECIALISTS." Scientific Journal of Polonia University 43, no. 6 (2021): 80–88. http://dx.doi.org/10.23856/4310.

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The article presents the results of the analysis of alternative methods of studying theGood Pharmaceutical Practice complex, introduced at the Lviv Polytechnic National University.The optimal structure of the curriculum for student’s education by the specialty 226 “Pharmacy,Industrial Pharmacy” was determined to improve the system of training of specialists,who need understand the current pharmaceutical legislation of Ukraine and prospects for itsdevelopment.Structural-and-logical schemas based on the Guidelines of Good Pharmaceutical Practicesthat greatly facilitate students’ perception and a
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Kendi, Njeri Nyambura. "Impact of Regulatory Reforms on Pharmacy Practice in Uganda." NEWPORT INTERNATIONAL JOURNAL OF SCIENTIFIC AND EXPERIMENTAL SCIENCES 5, no. 3 (2024): 22–25. http://dx.doi.org/10.59298/nijses/2024/10.5.322257.

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Access to safe and effective medicines is crucial for public health, particularly in low-resource settings like rural Uganda. Regulatory reforms in Uganda's pharmaceutical sector have aimed to enhance pharmacy practice, medication safety, and compliance with international standards. Recent amendments to the Pharmacy and Drugs Act have strengthened oversight, requiring pharmacies to adhere to Good Pharmacy Practice (GPP) guidelines for improved medication dispensing and storage. Challenges persist, including resource constraints and uneven enforcement across regions, impacting compliance and qu
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Cardins, Karla Karolline Barreto, Claudia Helena Soares de Morais Freitas, and Gabriela Maria Cavalcanti Costa. "Medicine dispensation in the prison system: Is pharmaceutical care assured?" Ciência & Saúde Coletiva 27, no. 12 (2022): 4589–98. http://dx.doi.org/10.1590/1413-812320222712.13092022en.

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Abstract This paper aims to analyze the process of medicine dispensation in prisons. A qualitative study was conducted in seven penitentiaries in Paraíba with 13 health professionals and 43 people deprived of liberty using essential/strategic medicines from February to August 2016. The results were categorized from the perspective of Bardin’s content analysis. Three categories emerged: medicine storage location in the prison system, delivery process in the prison system, and health-related responsibilities with pharmaceutical care. We can conclude that the lack of pharmacies, the legal non-com
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Giwangkara, I. Gusti Agung Ayu Ningrat, Dewa Ayu Putu Satrya Dewi, I. Gusti Ngurah Mayun, and Ni Putu Aryati Suryaningsih. "Evaluation Of Medicine Storage Management and Compatibility With Storage Standards in The Pharmaceutical Warehouse of Hospital Badung Regency." Pharmacon: Jurnal Farmasi Indonesia 20, no. 2 (2023): 205–15. http://dx.doi.org/10.23917/pharmacon.v20i2.23309.

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The effectiveness of drug storage is essential for effective drug management; if it is inadequate, pharmacy services and performance will be compromised. Therefore, a review of drug storage management and the appropriateness of drug storage regulations is required. The purpose of this study was to evaluate the effectiveness of drug storage and the acceptability of drug storage in the pharmaceutical warehouse of Hospital, Badung Regency. This study used cross-sectional methodology, descriptive observational quantitative research, and data collected from all medicinal products between March and
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Aher, Kalyani J., Dr Rishikesh S. Bacchav, and Prof Smita S. Aher. "Impurities in Pharmaceutical Substances." International Journal of Pharmaceutical Research and Applications 10, no. 1 (2025): 562–69. https://doi.org/10.35629/4494-1001562569.

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The quality, safety, and effectiveness of pharmaceutical products are significantly impacted by impurities in active pharmaceutical ingredients (APIs). During the synthesis, production, and storage processes, these impurities may originate from a number of sources, such as pollutants, reagents, residual solvents, and degradation products. International regulatory bodies including the FDA, EMA, and ICH strictly control the presence of impurities in APIs and offer detailed recommendations on permissible impurity levels and testing procedures. For the detection and measurement of contaminants, an
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Osyntseva, Alina. "Administration of Drugs for Pharmacotherapy of Tuberculosis According to GSP Requirements." SSP Modern Pharmacy and Medicine 4, no. 2 (2024): 1–17. http://dx.doi.org/10.53933/sspmpm.v4i2.140.

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This research paper outlines the findings from a comprehensive investigation focused on the dispensation and management of antituberculosis medications in pharmaceutical practices. The examination of antituberculosis medications was conducted using various classification systems, including ATC codes, clinical and pharmacological, classification and legal, nomenclature and legal groups. The study provides a detailed analysis of the harmonization process for GxP standards within Ukraine, offering a thorough understanding of the current practices. Additionally, the research looks into the supply
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Gerrans, James, Parastou Donyai, Katherine Finlay, and R. Simon Sherratt. "An Efficient Smart Pharmaceutical Packaging Technology Framework to Assess the Quality of Returned Medication through Non-Intrusively Recording Storage Conditions after Dispensation." Technologies 11, no. 3 (2023): 75. http://dx.doi.org/10.3390/technologies11030075.

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Medicine waste is a global issue, with economic, environmental, and social consequences that are only predicted to worsen. A structured review of the literature on medicine reuse revealed that there is a lack of technological applications addressing the key concerns raised by pharmaceutical stakeholders on the safety and feasibility of redispensing medication. A basis and guidelines for solutions aiming at enabling medicine reuse were devised by exploring a conceptual model of a Circular Pharmaceutical Supply Chain (CPSC), discussing concerns raised within the literature and identifying method
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Listiana, Wahyu, and Rochana Ruliyandari. "Analisis manajemen logistik farmasi di Rumah Sakit Jiwa Grhasia Yogyakarta." International Journal of Healthcare Research 3, no. 1 (2020): 1–11. http://dx.doi.org/10.12928/ijhr.v3i1.6498.

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Hospital Pharmacy Installation (IFRS) is a hospital unit as a place to carry out drug management activies. Pharmaceutical logistics management is the process of managing hospital pharmaceutical preparations ranging from planning, budgeting, procurement, storage, distribution, recording and reporting well as drug destruction in accordance with standard operating procedures. In the pharmacy installation of Yogyakarta Grhasia Mental Hospital have experienced drug vacancies in pharmaceutical logistics warehouses caused by empty stock of medicines from factories and the e- catalog process which is
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Hodgar, Sachin K., and Sumit R. Deore. "“Development And Validation Of An Rp-Hplc Method For Estimating Process-Related Impurities In Antidiabetic Drugs”." International Journal of Environmental Sciences 11, no. 8s (2025): 978–86. https://doi.org/10.64252/0rpq4s64.

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There has been ever increasing interest in impurities present in Active Pharmaceutical Ingredient’s (API’s). Nowadays, not only purity profile but also impurity profile has become mandatory according to the various regulatory authorities. The study aimed to develop and validate a reverse-phase high-performance liquid chromatography (RP-HPLC) method for the simultaneous estimation of process-related impurities in Dapagliflozin, Vildagliptin, and Sitagliptin. The method was optimized using various mobile phases and validated according to ICH guidelines for parameters including linearity, accurac
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Chandrasena, Pramila, Sampath Gunawardena, and Shanika Karunanayaka. "Storage, Disposal, and Misuse of Unused and Expired Pharmaceuticals in Households amongst Staff Working at Dakshinapaya Ministry Complex, Labuduwa, Galle Region: A Qualitative Phenomenological Study." Pharmacoepidemiology 3, no. 4 (2024): 314–35. http://dx.doi.org/10.3390/pharma3040022.

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(1) Background: Although Sri Lanka is a developing country and boasts of having a well-established healthcare system along with good healthcare indices, we are still lagging in certain aspects of healthcare. One such aspect is the deficiencies in guidelines and practices related to the handling of pharmaceutical waste. (2) Methods: This was a qualitative study performed using in-depth interviews with the help of a semi-structured questionnaire conducted among staff who are working at a ministry complex in Galle, Sri Lanka. Data analysis was performed using thematic analysis, (3) Results: There
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Vlasenko, I. O., and L. L. Davtian. "Pharmaceutical care for patients with diabetes: storage of insulin." Farmatsevtychnyi zhurnal, no. 5 (October 29, 2019): 21–34. http://dx.doi.org/10.32352/0367-3057.5.19.03.

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According to statistics, 1.2 million Ukrainians suffer from diabetes, and 201626 people being registered and requiring insulin (PI). In Ukraine, a system of reimbursement is introduced, which provides for the dispatch of PI from pharmacies. Thus, in the process of providing patients with diabetes with insulin, pharmacies play a significant role and, accordingly, provide them with pharmaceutical assistance. Insulin is used to treat both type 1 and type 2 diabetes mellitus. Successful treatment requires confidence that the insulin will work properly. Improper storage can lead to a decrease in in
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Daly, Liz. "The Effects of Current Cold Chain Management Equipment in Controlling the Temperature of Pharmaceutical Stores in an Australian Defence Force Exercise Environment." Prehospital and Disaster Medicine 34, s1 (2019): s124. http://dx.doi.org/10.1017/s1049023x1900267x.

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Aim:The purpose of this pilot study was to analyze the current cold chain storage methods of Class 8 stores, specifically thermolabile medications and temperature sensitive diagnostics, dressings, and fluids, for the Australian Army in a training area within Australia. This research was designed to identify deficiencies in current storage methods, including the inability to maintain the recommended storage temperature of pharmaceutical stores in accordance with the Therapeutic Goods Administration, as well as foster communication between key stakeholders, including the Royal Australian Army Me
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Adullahi, Abba Khalid, Adeniji Kehinde Olowosulu, and T. S. Allagh. "QUALITY ASSESSMENT AND STABILITY STUDIES OF METRONIDAZOLE TABLETS FORMULATIONS OBTAINED VIA CRYSTALLO CO-AGGLOMERATION TECHNIQUE." FUDMA JOURNAL OF SCIENCES 8, no. 3 (2024): 81–90. http://dx.doi.org/10.33003/fjs-2024-0803-2273.

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Stability studies are essential for assessing the quality, safety, and efficacy of pharmaceutical products, ensuring they maintain their properties over time. This study aimed to assess the stability of metronidazole tablets stored in a desiccator with charged silica gel following the International council for harmonization of Technical Requirements for Pharmaceuticals for Human Use guidelines. Metronidazole tablets were formulated from metronidazole co-agglomerates using different excipients by direct compression method and stored for 6 and 12 months at 25±2°C/60±5% relative humidity. Quality
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Sarif, Niroush Konari, T. Jacob Jane, and Prakash Vipin. "Stability Indicating UV Spectrophotometric Method For Linagliptin and Metformin in Pharmaceutical Dosage Form." Pharmaceutical Methods 8, no. 2 (2017): 01–06. https://doi.org/10.5281/zenodo.14855540.

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Introduction: Linagliptin and metformin are newly introduced FDA drug combination for the treatment type 2 diabetic patients.This study reveals the development of three methods for the UV spectrophotometric simultaneous estimation of linagliptin and metformin in pharmaceutical dosage and forced degradation studies on four different stress conditions. Methods: Development of method was based upon simultaneous equation,absorbance ratio and absorbances correction method with a simple solvent system of distilled water. Absorption maxima was found to be 230.4nm, 294.4nm for metformin and linoglipti
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SYAFITRI, FIYA DINDA, and YULIAWATI YULIAWATI. "STORAGE MANAGEMENT OF NARCOTICS AND PSYCHOTROPIC DRUGS." International Journal of Prevention Practice and Research 02, no. 06 (2022): 01–05. http://dx.doi.org/10.55640/medscience-abcd617.

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The storage management of narcotics and psychotropic drugs is a critical aspect of pharmaceutical practice, encompassing a set of stringent guidelines and protocols designed to ensure the safety, security, and regulatory compliance of these controlled substances. This abstract provides an overview of the key considerations in the storage of narcotics and psychotropic drugs, focusing on the challenges faced by healthcare professionals, regulatory frameworks governing storage practices, and emerging technologies that contribute to enhanced storage management. The article delves into the specific
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Nelwan, Olga Enggelina, Alexander Sam Leonard Bolang, and Vennetia Ryckerens Danes. "Evaluation Of Medicine Management at the UPTD Pharmacy Warehouse Manembo-Nembo Hospital Type C Bitung." Lead Journal of Economy and Administration 2, no. 1 (2023): 1–10. http://dx.doi.org/10.56403/lejea.v2i1.118.

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This study was conducted to determine how to evaluate drug management in the pharmaceutical warehouse of the UPTD Manembo-Nembo Hospital type C Bitung. This research uses qualitative research methods by conducting in-depth interviews, document review and observation. This research was conducted at the Pharmacy Warehouse of UPTD Manembo-nembo Hospital Type C Bitung which is located at Jalan SH Sarundajang, Manembo-nembo Tengah Village, Matuari District, Bitung City, North Sulawesi from April to June 2023. The informants of this research are those who have the authority to manage drugs in the Ph
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Rost, Johanna, Steve Langhein, Detlef Bartel, Andreas Bonertz, and Vera Mahler. "Good manufacturing practice- and good distribution practice-compliant cold storage and refrigerated transport of allergen products: what is important?" Allergo Journal International 31, no. 2 (2021): 36–42. http://dx.doi.org/10.1007/s40629-021-00193-3.

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Abstract Background All currently available products for diagnosis and therapy of type I allergies are protein extracts from allergenic source material. The extracted proteins have different properties and their structure is differently labile to temperature variations. Despite various pharmaceutical formulations to increase product stability, with few exceptions, allergen products must be refrigerated to ensure that their quality and native protein structure do not change during storage and transport. Maintaining quality is a challenge in complex distribution chains. Methods Regulatory requir
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Pratama, Muhammad Ihsan, Muhammad Syamsu Hidayat, and Rochana Ruliyandari. "Analisis Pengelolaan Logistik Farmasi di Instalasi Farmasi RSUD Raden Mattaher Selama Pandemi Covid-19." Syntax Literate ; Jurnal Ilmiah Indonesia 8, no. 10 (2023): 5841–58. http://dx.doi.org/10.36418/syntax-literate.v8i10.13778.

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The efficiency of the pharmaceutical logistics management process can indirectly affect the balance of pharmaceutical supplies in hospitals. The aim of this research is to analyze the management of pharmaceutical logistics at Raden Mattaher Regional Hospital, Jambi Province during the Covid-19 pandemic. The method used in this research is descriptive qualitative using a phenomenological approach. The variables looked at include selection, planning, budgeting, procurement, storage and distribution. Data collection in this research was carried out by means of observation, in-depth interviews, an
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Vardan, Victor. "Influence of pH on the Stability of Pharmaceutical Compounds in Japan." Journal of Chemistry 3, no. 2 (2024): 21–30. http://dx.doi.org/10.47672/jchem.2404.

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Purpose: The aim of the study was to assess the influence of pH on the stability of pharmaceutical compounds in Japan. Methodology: This study adopted a desk methodology. A desk study research design is commonly known as secondary data collection. This is basically collecting data from existing resources preferably because of its low cost advantage as compared to a field research. Our current study looked into already published studies and reports as the data was easily accessed through online journals and libraries. Findings: The study showed that the ionization state of a drug molecule can c
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Mavungu Landu, Don Jethro, Michel Frédérich, Joseph Manzambi Kuwekita, et al. "Quality of antimalarials in Kinshasa peri-urban areas with regard to local pharmaceutical legislation and regulation." International Health 12, no. 4 (2019): 253–63. http://dx.doi.org/10.1093/inthealth/ihz070.

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Abstract Background In the context of old pharmaceutical legislation and regulations not adapted to current realities, the aim of the present study was to evaluate the existing pharmaceutical system in peri-urban areas of Kinshasa. Methods A prospective study was carried out during the period 2016–2018. The most used antimalarial medicines were identified through household and pharmaceutical establishment surveys. The samples of the obtained medicines were assayed with generic separation methods using the high-performance liquid chromatography technique coupled to a diode array detector. The r
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Riady, Ninda Thiara, Nurlina Nurlina, and Vina Purnamasari. "Gambaran Pengelolaan Obat Di Instalasi Farmasi Rsud Provinsi Sulawesi Barat." Makassar Pharmaceutical Science Journal (MPSJ) 2, no. 1 (2024): 53–65. https://doi.org/10.33096/mpsj.v2i1.144.

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Hospital Pharmacy Installation (IFRS) is a functional implementing unit organizes all pharmaceutical service activities in hospitals, which functions to carry out the management of pharmaceutical supplies with the stages of selecting, planning, procuring, storing, distributing, controlling, deleting, recording and reporting. This study aims to determine the stages of management of pharmaceutical supplies in West Sulawesi Provincial Hospital using descriptive qualitative research through interviews and observation (observation). In this study guided interviews that have been arranged systematic
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Wandira, Bertin Ayu, and Marsanda Chikita. "Implementation of Drug Logistics Management in Pharmaceutical Installations in Sigi Regency Health Office." Journal of Health and Nutrition Research 1, no. 2 (2022): 103–10. http://dx.doi.org/10.56303/jhnresearch.v1i2.33.

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Drug logistics management at the health office is one of the important aspects of the Public Health Center. The purpose of the study was to determine the planning, budgeting of procurement, storage, distribution, and elimination in drug logistics management at the Pharmacy Installation of the Sigi Regency Health Office. This type of research was qualitative with a case study approach. The informants in this study consisted of key informants (the Head of the Pharmacy Installation of the Sigi Regency Health Office), the usual informants (the Pharmacy Installation Staff of the Sigi Regency Health
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Abushal, S. A., H. Uguru, O. Akpomedaye, et al. "Effect of storage conditions on the dietary and pharmaceutical values of ginger oil, and modeling its dielectric properties." Grasas y Aceites 75, no. 4 (2024): 2207. https://doi.org/10.3989/gya.1200232.2207.

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This research was conducted to evaluate the impact of the storage conditions of ginger rhizomes on the nutritional and therapeutic properties of the ginger oil (GO). The physicochemical and phytochemical properties, fatty acid contents and dielectric constant (ε′) of the GO were analyzed in accordance with standard guidelines. The findings revealed that the storage temperature significantly impacted the quality of GO (p < 0.05). Notably, the oil contains a significant amount of acid value (AV), free fatty acid (FFA), saponification value (SV), iodine value, vitamin C, phenolic compounds, an
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Binson, Guillaume, Karine Beuzit, Virginie Migeot, et al. "Preparation and Physicochemical Stability of Liquid Oral Dosage Forms Free of Potentially Harmful Excipient Designed for Pediatric Patients." Pharmaceutics 11, no. 4 (2019): 190. http://dx.doi.org/10.3390/pharmaceutics11040190.

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Dexamethasone, hydrochlorothiazide, spironolactone, and phenytoin are commonly used in neonates, but no age-appropriate formulation containing these active pharmaceutical ingredients (APIs) is commercially available. Thus, pharmaceutical compounding of the liquid oral dosage form is required to enable newborn administration. A problem common to the compounded preparations described in the literature is that they include potentially harmful excipients (PHEs). Therefore, the aim of this study was to evaluate the feasibility of compounding oral liquid dosage forms free of PHE, containing dexameth
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Jannatun Nisa, Nicky Saputra, and Nor Latifah. "Uji Stabilitas Obat Sediaan Tablet: Prinsip, Pedoman ICH Q1, dan Parameter Kritis." OBAT: Jurnal Riset Ilmu Farmasi dan Kesehatan 3, no. 4 (2025): 88–94. https://doi.org/10.61132/obat.v3i4.1507.

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This article provides a comprehensive review of drug stability testing, specifically focusing on tablet dosage forms. It elucidates the fundamental principles, the critical role of ICH Q1 guidelines, and essential parameters evaluated during stability studies, including physical, chemical, and microbiological aspects. The discussion covers various types of stability studies, standardized storage conditions, and the interpretation of results for determining shelf life and ensuring product quality. Relevant case studies on tablet stability are also integrated to illustrate practical applications
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36

Mansi, P. Rana. "Overview Of Degradation Studies For Pharmaceutical Drug Candidates." International Journal in Pharmaceutical Sciences 2, no. 4 (2024): 193–211. https://doi.org/10.5281/zenodo.10913401.

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Degradation studies play a crucial role in the pharmaceutical industry, offering invaluable insights into the stability, safety, and efficacy of drug candidates. This review article provides a comprehensive overview of the methodologies, challenges, and recent advancements in degradation studies aimed at evaluating the stability profiles of pharmaceutical compounds. The review begins by outlining the importance of degradation studies in drug development, emphasizing their significance in predicting the shelf-life and establishing the quality attributes of drug products. Various factors influen
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Erviana, Erna, Yulian Wahyu Permadi, Wulan Agustin Ningrum, and Ainun Muthoharoh. "Evaluasi Pengelolaan Sediaan Farmasi dan Bahan Medis Habis Pakai Pada Puskesmas di Kabupaten Pekalongan Berdasarkan Petunjuk Teknis Standar Pelayanan kefarmasian di Puskesmas Tahun 2019." Prosiding Seminar Nasional Kesehatan 1 (November 17, 2021): 117–27. http://dx.doi.org/10.48144/prosiding.v1i.634.

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AbstractManagement of pharmaceutical preparations is a series of activities involving aspects of planning, procurement, receipt, storage, distribution, destruction and withdrawal, control and administration of drugs that are managed optimally to ensure the achievement of determination of the amount and type of pharmaceutical supplies. The purpose of this study was to evaluate the management of pharmaceutical preparations and medical consumables in health centers in Pekalongan Regency based on the Technical Instructions for Pharmaceutical Services at Puskesmas in 2019. The method used in this s
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Rajat, Vaishnav, and S. Ranawat Mahendra. "Stability Testing of Ayurvedic Drugs: An Indian Regulatory Perspective." Pharmaceutical and Chemical Journal 9, no. 5 (2022): 1–10. https://doi.org/10.5281/zenodo.13973346.

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he safety and effectiveness of a product are greatly influenced by its stability. Ayurvedic, Siddha, and Unani (ASU) medicine includes single-herb or polyherbal formulations with or without mineral medications and/or drug ingredients derived from animals. Pharmaceutical products have currently undergoing stability testing in accordance with the guidelines of the International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH). The First Schedule of the Drugs and Cosmetics Act, 1940 includes a concept of shelf l
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Rizky Subagya, Kamiel Roesman Bachtiar, and Ayu Rahmawati. "Analisis Pengelolaan Obat Di Puskesmas Cibalong Kecamatan Cibalong Tahun 2022 Berdasarkan Permenkes Ri Nomor 74 Tahun 2016." Termometer: Jurnal Ilmiah Ilmu Kesehatan dan Kedokteran 1, no. 4 (2023): 227–38. https://doi.org/10.55606/termometer.v1i4.2466.

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Drug management at the puskesmas is an activity that includes planning needs, requests, receipts, storage, distribution, control, recording, reporting, archiving as well as management monitoring and evaluation. Drug management that is not ideal can be caused by drug planning that is only based on previous year's estimates, as well as inadequate facilities for the process of storing and distributing drugs. One way to overcome drug management that is not ideal is to compare the management of drugs at the health center with Permenkes number 74 of 2016 concerning pharmaceutical service standards a
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40

Diana, Khusnul, Nur Ekasandra, and Muhamad Rinaldhi Tandah. "EVALUASI PENYIMPANAN DAN PENDISTRIBUSIAN VAKSIN COVID-19 DI DINAS KESEHATAN PROVINSI SULAWESI TENGAH." Jurnal Insan Farmasi Indonesia 6, no. 3 (2024): 40–52. http://dx.doi.org/10.36387/jifi.v6i3.1657.

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The Health Department is responsible for distributing COVID-19 vaccines in the region. This research was conducted to evaluate the suitability of storage and distribution in the warehouse of the Pharmaceutical Installation of the Central Sulawesi Health Department, following the guidelines set in the Director General of Disease Prevention and Control Decision Number Hk.02.02/4/1/2021. The research used observational and qualitative descriptive methods, collecting data within a specific period, using all COVID-19 vaccines stored in the Pharmaceutical Installation of the Central Sulawesi Health
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Charoo, Naseem A., Omotayo Akanji, Ziyaur Rahman, Aqeel A. Khan, and Aqal Badshah. "Risk-Based Approach for Defining Retest Dates for Active Pharmaceutical Ingredients and Excipients." Pharmaceuticals 17, no. 7 (2024): 903. http://dx.doi.org/10.3390/ph17070903.

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Drug substances and excipients must be stored in recommended storage conditions and should comply with their specifications during the retest period for their use in the manufacture of drug products. The ICH (International Council for Harmonization of Technical Requirements for Pharmaceuticals for Human Use) and WHO (World Health Organization) regulatory guidelines mandate that after the retest period, the drug substances must be retested for compliance with the specification and then used immediately in the manufacture of the finished product. Although these substances can be retested multipl
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Bellich, Barbara, Martina Franzin, Debora Curci, et al. "Long-Term Stability of Glycopyrrolate Oral Solution Galenic Compound at Different Storage Conditions." Pharmaceutics 16, no. 8 (2024): 1018. http://dx.doi.org/10.3390/pharmaceutics16081018.

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Glycopyrrolate is a competitive muscarinic receptor antagonist used in the treatment of sialorrhea, especially in pediatrics. Degradation research was conducted to better understand the stability of the active pharmaceutical ingredient (API). Using an HPLC-UV method, we evaluated the chemical stability of the oral solution of the galenic compound glycopyrrolate 0.5 mg/mL under different storage conditions. Method validation was performed according to the International Council for Harmonization (ICH) Q2(R2) guidelines. The results of the stability study of the galenic compound in different stor
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Wuri Ariestika Sari and Eri Amalia. "Evaluasi Pengelolaan Produk Rantai Dingin pada Pedagang Besar Farmasi X Berdasarkan Pedoman CDOB 2020." OBAT: Jurnal Riset Ilmu Farmasi dan Kesehatan 2, no. 5 (2024): 136–44. http://dx.doi.org/10.61132/obat.v2i5.670.

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Cold Chain Products are pharmaceutical preparations sensitive to temperature, requiring consistently maintained temperature conditions from production, storage, and transportation to the final consumer. Environmental changes, such as temperature fluctuations and direct sunlight exposure, can reduce product quality, leading to the loss of the product's therapeutic potential. Therefore, Pedagang Besar Farmasi (PBF) play a crucial role throughout the distribution chain of cold chain products to ensure that the quality and effectiveness of the products are maintained. This study aims to evaluate t
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Rawas, Ghufran M., Shahad F. AlAhmadi, and Ahmad H. Mufti. "Evaluation of public knowledge and attitude towards how to use, store and discard expired pharmaceutical drugs in Saudi Arabia." International Research Journal of Medicine and Medical Sciences 9, no. 3 (2021): 103–12. http://dx.doi.org/10.30918/irjmms.93.21.022.

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This study aimed to evaluate the public knowledge and attitude toward how to use, store and discard unused and expired pharmaceutical drugs among the Saudi population. A descriptive cross-sectional study design was used to evaluate the knowledge, attitude, and practice of participants toward the usage and disposal of expired pharmaceutical products among the Saudi population via an online survey distributed throughout social media sites during the period of two months from March 2020 to May 2020. Microsoft Excel and graph pad software analyzed the cleaned data. Descriptive statistics on sample
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Xiang, Shuanglin, Wenyong Gao, Haining Peng, et al. "Standards of clinical-grade mesenchymal stromal cell preparation and quality control (2020 China Version)." Journal of Neurorestoratology 8, no. 4 (2020): 197–216. http://dx.doi.org/10.26599/jnr.2020.9040021.

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Mesenchymal stromal cells (MSCs) including mesenchymal stem cells to potentially differentiate into different tissue lineages widely exist in various tissues. In recent years, the clinical research and application of MSCs have become more extensive, but no standardized guidelines for the preparation and quality control of clinical-grade MSCs currently exist. To standardize the preparation and quality control of MSCs using the human umbilical cord, placenta, bone marrow, and adipose tissue as sample sources for the Chinese Association of Neurorestoratology (CANR; Preparatory) and the China Comm
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Prawenti, Herlita, Ria Miftakhul Jannah, Ali Murtopo, Fajar Susilowati, and Annisa Wiji Septianingsih. "Training on the assessment of the building functions’ feasibility for Dukunan Village community." Community Empowerment 9, no. 2 (2024): 258–65. http://dx.doi.org/10.31603/ce.10582.

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The Dukunan Hamlet community encompasses various buildings, including a mosque, prayer room, and village inventory storage facility, which are generally utilized. However, specific areas within these buildings require prioritized treatment to ensure their functional feasibility. This community service program aims to enhance community understanding and awareness regarding the functional suitability of buildings to support village development and community independence. The method employed to achieve these objectives involves conducting counseling and assessment training utilizing the guideline
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47

Hotha, Priyanka P., and Purvi J. Tanna. "An audit of drug package insert: a survey based study in India." International Journal of Basic & Clinical Pharmacology 6, no. 3 (2017): 629. http://dx.doi.org/10.18203/2319-2003.ijbcp20170826.

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Background: The primary source of drug information is a Package Insert. It is a printed leaflet that contains information based on regulatory guidelines for the safe and effective use of a drug. It is also known as prescription drug label or prescribing information. Regulatory requirements for drug package inserts or leaflets vary across nations. United States-Food and Drug Administration (US-FDA) and European Medicines Agency (EMA) amend their regulations governing the content and format of labelling for drug products from time to time. US-FDA has published a revised guideline in the Federal
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48

Ortega, Raquel, Natalia Navas, Antonio Salmerón, José Cabeza, and Luís F. Capitán-Vallvey. "Validated Stability-Indicating HPLC Method for Paricalcitol in Pharmaceutical Dosage Form According to ICH Guidelines: Application to Stability Studies." Journal of AOAC INTERNATIONAL 94, no. 2 (2011): 543–49. http://dx.doi.org/10.1093/jaoac/94.2.543.

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Abstract A stability-indicating HPLC method with diode array detection for the determination of paricalcitol, a synthetic vitamin D2 analog, was developed. Analytical parameters were studied according to International Conference on Harmonization guidelines. A C18 column (250 4.6 mm, 5 m particle size) maintained at 25C was used as the stationary phase, and acetonitrilewater (70 30, v/v) as the mobile phase. Chromatograms were recorded at 250 nm. In forced degradation studies, the effects of acid, base, oxidation, temperature, and UV light were investigated and showed no interference with the d
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Yanti, Sari, and Misa Ayu Lia Sari. "Kesesuaian Penyimpanan Vaksin Covid-19 Di Instalasi Farmasi Di Salah Satu Dinas Kesehatan Bengkulu." Jurnal Vokasi Kesehatan 3, no. 1 (2024): 1–8. http://dx.doi.org/10.58222/juvokes.v3i1.366.

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Vaccine management is an inseparable part of service. Every service unit must manage vaccines properly according to vaccine management guidelines as a quality of service. Vaccines which are included in freeze sensitive vaccines and heat sensitive vaccines, if not stored at the perfect temperature, can cause loss of vaccine potency. The purpose of this study was to review how the Covid-19 vaccine preparations were stored at the Bengkulu Health Office. This research uses an observational design with a checklist & interview method for retrospective data collection with a cross sectional appro
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Kovacic Krizanic, Katarina, Florian Prüller, Konrad Rosskopf, Jean-Marc Payrat, Silke Andresen, and Peter Schlenke. "Preparation and Storage of Cryoprecipitate Derived from Amotosalen and UVA-Treated Apheresis Plasma and Assessment of In Vitro Quality Parameters." Pathogens 11, no. 7 (2022): 805. http://dx.doi.org/10.3390/pathogens11070805.

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Cryoprecipitate is a plasma-derived blood product, enriched for fibrinogen, factor VIII, factor XIII, and von Willebrand factor. Due to infectious risk, the use of cryoprecipitate in Central Europe diminished over the last decades. However, after the introduction of various pathogen-reduction technologies for plasma, cryoprecipitate production in blood centers is a feasible alternative to pharmaceutical fibrinogen concentrate with a high safety profile. In our study, we evaluated the feasibility of the production of twenty-four cryoprecipitate units from pools of two units of apheresis plasma
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