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Publication Years
1502
3841
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35
2
1
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507
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76
1
Toolboxes
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564
520
311
298
257
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6th edition
Аудіометрія у веденні випадків туберкульозу із резистентністю до протитуберкульозніх препаратів
Mamel Quelapio, Maria Idrissova, Gunta Dravniece et al.
USAID, KNCV Tuberculosis Foundation, Challenge TB
(2017)
C2
Дане руководcтво призначене для медіцінcкіх працівників іcпользующіх аудіометрію для прийняття обоcнованних рішень, орієнтованих на пацієнта для профілактики і л
...
кування ототокcічноcті, являющейcя результатом іcпользованія ін'єкційних препаратів другого ряду (ІПВР).
more
Руководящие принципы для интенсивного выявления туберкулеза и профилактической терапии изониазидом у людей, живущих с ВИЧ, в условиях нехватки ресурсов
World Health Organization
Департамент по ВИЧСПИД, Департамент «Остановить ТБ», Всемирная организация здравоохранения
(2011)
C_WHO
В этих новых руководящих принципах рекомендуется использовать упрощенный алгоритм скрининга, основанного на четырех клинических симптомах, для выявления
...
иц, которым показана либо ПТИ, либо дальнейшая диагностика для выявления ТБ и других заболеваний.
more
Обратим вспять эпидемии ВИЧ и туберкулеза
Глобальный фонд для борьбы со СПИДом, туберкулезом и малярией
Глобальный фонд для борьбы со СПИДом, туберкулезом и малярией
(2019)
C1
Руководство по инвестициям Глобального фонда для стран Восточной Европы и Центральной Азии. В ходе разработки Руководства Глобальный фонд стремился учесть мнени
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всех значимых участников борьбы с эпидемиями ВИЧ-инфекции и туберкулеза в Восточной Европе и Центральной Азии и с этой целью провел ряд консультаций и рабочих встреч с широким кругом заинтересованных сторон, на которых обсуждались цели и принципы дифференцированного подхода к противодействию эпидемиям в регионе, а также механизмы реализации этих целей и принципов.
Accessed on 2019
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Accessed:10.03.2020
South African National TB Guidelines - Children
Medicines Information Centre; SPES Bona; National HIV & TB Health Care Worker Hotline
Medicines Information Centre; SPES Bona; National HIV & TB Health Care Worker Hotline
(2019)
C2
Accessed: 08.10.2019
Based on the National Guidelines for the Management of Tuberculosis in Children 2013, Department of Health, South Africa.
Technical package for cardiovascular disease management in primary health care.
The primary role of Benin’s Department of Pharmacy and Medicines (DPMED) is to develop and apply the national pharmaceutical policy. The main objective of this policy is to ensure the availability and accessibility of quality medicines for the population. To fulfill its mandate, DPMED aims to stre
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ngthen its regulatory capacity, including the issuance of licenses to pharmaceutical establishments and the registration of pharmaceutical products. Benin’s current registration system shares core concerns that are common to most developing countries, notably the capacity to evaluate and monitor the security, efficacy, and quality of medicines and other health products. It is currently characterized by 1) poor or inadequate traceability of records or regulations (example: a product’s marketing authorization [MA] is often hard to find); 2) lack of evidence used in the regulatory decision-making process (reasons behind special import authorization, i.e., products without valid MAs); 3) inconsistent and unsecured archiving system; 4) limited human resources; and 5) an inefficient information management system
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In September, 2018, the first international Medicine Quality and Public Health Conference was held at Oxford University, UK, to discuss opportunities and solutions to ensure that all people have access to affordable and quality-assured medical products. Delegates developed the short Oxford Statement
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, calling for investment, policy change, and action to eliminate substandard and falsified medical products. The statement was born out of discussion between governments, national and international agencies, non-governmental organisations, professional associations, and academic institutions who together examined the latest evidence on the epidemiology and public health implications of substandard and falsified medical products.
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This implementation tool describes the recommended approaches for routine monitoring of toxicity integrated with the national monitoring and evaluation system and targeted approaches to monitoring toxicity to enable enhanced monitoring and reporting of treatment-limiting toxicity to support country
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implementation and generation of local data.
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