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1
Publication Years
2104
4616
666
30
4
1
1
Category
2880
518
489
461
457
177
66
3
Toolboxes
712
418
414
407
318
255
241
223
209
201
165
154
147
131
114
107
83
79
73
66
61
33
29
26
25
3
2
National Tuberclosis and
Leprosy Programme (NTLP)
NATIONAL TUBERCULOSIS AND LEPROSY PROGRAMME
Essential Drug list on page 36!!
Integration of EPI and paediatric HIV services for improved ART initiation in Zimbabwe
M. Prescott, C. Boeke, T. Gotora, et al.
International Initiative for Impact Evaluation (3ie)
(2017)
C1
The Interim Guidance on Cholera Rapid Diagnostic Tests (RDTs) by the Global Task Force on Cholera Control (GTFCC) provides recommendations for using RDTs to detect cholera in areas with limited laboratory capacity. It highlights the advantages of RD
...
Ts, such as rapid detection (within 30 minutes), ease of use by non-laboratory personnel, and their role in early outbreak identification and surveillance. However, it emphasizes that RDTs should not replace culture or PCR testing, as they vary in sensitivity (58-100%) and specificity (60-100%). The document advises on proper test selection, storage, training, and integration into national surveillance systems to enhance cholera response efforts.
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The essential medicines are those that meet the priority needs of the healthcare of the population. While reviewing the 5th edition of the essenti
...
al Medicines, special attention focused on the health sector policy. Indeed, medicines play an important role in protecting, maintaining and restoring the peoples’ health and credibility of health facilities. Their availability is a fundamental aspect of primary health care as defined in different declarations including Alma-Ata of 1978.
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Activity brief | Research Partners: Population Council, IntraHealth International, Avenir Health, Survey Warehouse, Ministry of Health and Social Services, and USAID/Namibia | Location: Andara, Nyangana, Oshikuku, Onandjokwe, and Tsumeb districts, N
...
amibia | Study Duration: April 2017–September 2018
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Namibia guideline for submission of applications for registration of pharmaceuticals for human use in common technical document format.