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Publication Years
1
4028
7398
1060
75
6
2
2
Category
4637
806
748
661
649
261
126
3
Toolboxes
1131
949
580
526
518
508
455
409
388
346
315
294
287
223
212
200
198
175
152
131
116
111
96
78
75
12
2
MMWR: Recommendations and Reports / Vol. 62 / No. 9
Morbidity and Mortality Weekly Report
October 25, 2013
Drug-Resistant tuberculosis
E.G. Brown Jr, D.S. Dooley, K. Smith
Curry International Tuberculosis Center, State of California, California Health & Human Service Agency, Department of Public Health
(2016)
C1
A survival guide for clinicans.
3rd edition.
Lineamientos para el Manejo Clínico y Operativo de la Tuberculosis Drogorresistente
J. A. Caminero, A. Van Deun, P. I. Fujiwara, et. al
Unión Internacional Contra la Tuberculosis y Enfermedades Respiratorias
(2013)
National Center for HIV/AIDS, Viral Hepatitis, STD, and TB Prevention.
Division of Tuberculosis Elimination.
The intent of these guidelines is to develop a holistic, coordinated, proactive and technology driven strategy for management of biological disasters through a culture of prevention, mitigation and preparedness to generate a prompt and effective response in the event of an emergency. Th
...
e document contains comprehensive guidelines for preparedness activities, biosafety and biosecurity measures, capacity development, specialised health care and laboratory facilities, strengthening of the existing legislative/
regulatory framework, mental health support, response, rehabilitation and recovery, etc. It specifically lays down the approach for implementation of the guidelines by the central ministries/departments, states, districts and other stakeholders, in a time bound manner.
more
First edition, November 1997 | Revised July 2002
PMPB/INS-GUIDE/01
PMPB/INS-GUIDE/04
Namibia guideline for submission of applications for registration of pharmaceuticals for human use in common technical document format.
Doc. No.: INS/GDL/001-(Annexes)
Medicines and Allied Substances [No. 3 of 2013 47 | An Act to continue the existence of the Pharmaceutical Regulatory Authority and re-name it as the Zambia Medicines Regulatory Authority; provide for the functions and powers of the Authority; provide for the registration and regulation of pharmacie
...
s, health shops and agro-veterinary shops; provide for the registration and regulation of medicines and allied substances; provide for the regulation of the manufacture, importation, exportation, possession, storage, distribution, supply, promotion, advertising, sale and use of medicines and allied substances; provide for the regulation and control of clinical trials; repeal and replace the Pharmaceutical Act, 2004; and provide for matters connected with, or incidental to, the foregoing.
more
Guidance for the preparation and submission of dossiers
Made under Section 5 (c) of the Tanzania Food, Drugs and Cosmetics Act, 2003 | Second Edition