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КОВИД-19 ХАЛДВАРЫН ОМИКРОНЫ ВА.5 ХУВИЛБАРЫН ҮЕИЙН ЭМНЭЛЗҮЙН ОНЦЛОГ

КОВИД-19 ХАЛДВАРЫН ОМИКРОНЫ ВА.5 ХУВИЛБАРЫН ҮЕИЙН ЭМНЭЛЗҮЙН ОНЦЛОГ

КОВИД-19 ХАЛДВАРЫН ДЕЛЬТА БОЛОН ОМИКРОНЫ ВА.1, ВА.2 ХУВИЛБАРЫН ЭМНЭЛЗҮЙН БАЙДЛЫГ ХАРЬЦУУЛСАН ДҮН

КОВИД-19 ӨВЧНИЙ ҮЕИЙН ВИРУСИЙН ЭСРЭГ ЭМИЙН ҮР НӨЛӨӨ, ЭРСДЭЛИЙН ҮНЭЛГЭЭ СУДАЛГААНЫ ДҮН

КОВИД-19-ИЙН ХАЛДВАРТАЙ ӨВЧТӨНҮҮДЭД МЭС ЗАСЛЫН ТУСЛАМЖ ҮЙЛЧИЛГЭЭ ҮЗҮҮЛСЭН БАЙДАЛ

КОВИД-19 ВИРҮСИЙН ХАЛДВАРЫН ЭМЧИЛГЭЭНД МОНГОЛЫН УЛАМЖЛАЛТ АНАГААХ УХААНЫ ЭМ БОЛОН ШИНЭЭР УРГАМЛЫН ГАРАЛТАЙ ЭМИЙГ ГАРГАН АВАХ СУДАЛГАА

КОВИД-19 ВАКЦИНЫ ГУРАВДУГААР ТУНГИЙН ДАРААХ ГЕМАТОЛОГИ, БИОХИМИ, КОАГУЛОГРАММЫН ШИНЖИЛГЭЭНИЙ ҮЗҮҮЛЭЛТҮҮДИЙГ ҮНЭЛСЭН ДҮН

КОВИД-19 ВАКЦИНЖУУЛАЛТ БОЛОН ХАЛДВАРЫН ДАРААХ SARS-COV-2 ВИРУСИЙГ СААРМАГЖУУЛАХ ИДЭВХИЙН СУДАЛГАА

Variable quality of dosage forms of a wide range of drugs has often been reported, prompting the WHO to set standards for generic products. This study aimed to assess the quality and dissolution characteristics of generic ciprofloxacin 500 mg products available on the market, by comparison with a leading brand as well as to establish dissolution profiles in order to inform manufacturers and decision makers. A post-marketing quality assessment and comparative dissolution study of five generic ciprofloxacin products from different manufacturers available in Mongolia were completed. USP buffer at pH=1.2 (hydrochloric acid solution) and pH=4.5 (phosphate buffer solution) were dissolution media. In addition, weight variation, hardness, friability, disintegration time and assay were determined according to established methods. All five sampled products complied with the official specifications for uniformity of weight, friability and disintegration time. All five samples contained >99% (w/w) of labeled chemical content. However, significant inter and intra-brand variabilities in terms of dissolution rate were detected. As only two generic ciprofloxacin tablets included in this investigation were similar with the chosen comparator brand, the study concludes that further in vivo investigations are required to assess their bioequivalence.

The history of modern pharmaceutical care in Mongolia began in 1923 when the first pharmacy in the country opened its doors. By the end of the 1980s, the pharmaceutical sector in Mongolia had evolved into a system, fully owned and strictly regulated by the state, with a focus on increasing the supply of medicines throughout the country, including every soum (sub-province administrative unit). In the early 1990s, a deep economic crisis and recession in Mongolia left the government unable to finance and maintain the operations of the vast pharmaceutical supply chain, leading to severe shortages of even the most essential medicines. The government introduced initial reforms that led to the privatization and liberalization of the pharmaceutical sector, which served the goal of eliminating the acute shortages in the supply of medicines in the 1990s. As a result of these initial reforms, the production and wholesale and retail distribution of medicines and medical devices are now entirely in the hands of the private sector. The initial reforms laid the foundation for the pharmaceutical sector in Mongolia as it currently stands and is the origin of the longer-term issues that persist in the sector and which undermine the safety and quality of medicines. With support from Asian Development Bank (ADB), the government is making significant progress in addressing these issues, including through (i) establishing a national medicines regulatory authority that consolidates previously fragmented regulatory functions, (ii) upgrading the national medicines safety laboratory to international standards, (iii) instituting good national pharmaceutical practices based on international standards, (iv) developing national strategies on pricing medicines and pharmacovigilance, and (v) introducing a system for the centralized procurement of medicines for public hospitals. These efforts have faced challenges, such as inadequate political support, lack of sustainable financing and investment options, and opposition from some stakeholders. Mongolia needs to transform the newly established national medicines regulatory authority into a more powerful, independent, evidence-based, and better funded institution that brings together disparate functions of different sectors. Improved regulation of medicines would ensure better quality and increased assurance of safety, covering areas such as pharmaceutical manufacturing, marketing, distribution, and inspection. All efforts to improve regulation of medicines in Mongolia must follow the implementation of a consistent policy, supported by improved coordination and collaboration with all stakeholders, including beneficiaries and, in particular, the private sector. This paper describes the pharmaceutical sector in Mongolia and ADB’s support for pharmaceutical sector reform, including the results of initial and ongoing reforms, challenges that remain, and future actions needed to ensure better regulation of medicines. The experience from ADB’s support for the reform of the pharmaceutical sector in Mongolia and the lessons learned will be useful for future programs in Mongolia and other countries.

ЦАР ТАХЛЫН НӨХЦӨЛД МОНГОЛ ХҮНИЙ ДАСАН ЗОХИЦОХ МЭДЛЭГ, ХАНДЛАГА, ДАДЛЫГ ТОГТООСОН ДҮН

ТОМУУ БОЛОН АМЬСГАЛЫН ЗАМЫН ЦОЧМОГ ХАЛДВАР ҮҮСГЭГЧДИЙН ТАНДАЛТЫН СУДАЛГАА

СУРГУУЛЬ, ЦЭЦЭРЛЭГИЙН АГААРЖУУЛАЛТЫН СИСТЕМИЙН ТӨЛӨВ БАЙДАЛД ХИЙСЭН ҮНЭЛГЭЭ

КОРОНАВИРУСТ ХАЛДВАР (КОВИД-19)-ЫН ЭСРЭГ ВАКЦИНЫ ТАЛААРХ ИРГЭД БОЛОН ЭРҮҮЛ МЭНДИЙН МЭРГЭЖИЛТНҮҮДИЙН МЭДЛЭГ, ХАНДЛАГА, ДАДЛЫГ ҮНЭЛСЭН ҮНЭЛГЭЭ

КОРОНАВИРУСТ ХАЛДВАР (КОВИД-19)-ЫН БУС ШАЛТГААНААР ЭМНЭЛЭГТ ХЭВТЭГСДИЙН ДУНД КОРОНАВИРУСТ ХАЛДВАР (КОВИД-19)-ЫН ЭСРЭГ ВАКЦИНЫ ДАРАА ИЛЭРСЭН УРВАЛ, ХҮНДРЭЛИЙГ ТАНДАХ СУДАЛГААНЫ УРЬДЧИЛСАН ДҮН

КОВИД-19 ЦАР ТАХЛЫН ҮЕИЙН ТОМУУ, ТОМУУ ТӨСТ ӨВЧИН (ТТӨ) ҮҮСГЭГЧДИЙН ТАНДАЛТ СУДАЛГАА

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