Filter
1989
Filtered Results: 1989
Text search:
registration
of
drugs
Featured
Recommendations
162
New Publications
656
Language
Document type
No document type
1300
Studies & Reports
254
Guidelines
216
Manuals
90
Strategic & Response Plan
76
Training Material
21
Fact sheets
16
Situation Updates
11
Resource Platforms
4
Brochures
1
Countries / Regions
India
193
Kenya
78
Uganda
54
Sierra Leone
51
Global
48
Ethiopia
48
Nigeria
47
South Africa
47
Nepal
45
Ghana
42
Tanzania
42
Bangladesh
41
Malawi
40
Rwanda
38
Liberia
35
Western and Central Europe
34
Myanmar / Burma
33
Namibia
29
Africa
28
Ukraine
27
Zambia
26
Latin America and the Carribbean
21
Philippines
19
Eastern Europe
19
Botswana
19
Cambodia
18
Syria
17
Zimbabwe
17
Lesotho
15
Asia
14
South–East Asia Region
14
Indonesia
14
South Sudan
13
Mozambique
11
Congo, Democratic Republic of
11
Eswatini/ Swaziland
8
Colombia
7
Tajikistan
6
Senegal
6
West and Central Africa
6
Sudan
6
Pakistan
6
East and Southern Africa
5
Moldova
5
Russia
5
Benin
4
Albania
4
Haiti
4
Venezuela
4
Jordan
4
Middle East and North Africa
4
Eastern Europe and Central Asia
4
Lebanon
4
Brazil
4
North Macedonia
3
Chile
3
Iran
3
Afghanistan
3
Germany
3
Paraguay
3
United Kingdom
3
Argentina
3
Sri Lanka
3
Georgia
3
Libya
3
Iraq
3
Timor Leste/ East Timor
2
Thailand
2
Cameroon
2
Laos
2
Burkina Faso
2
Armenia
2
Saudi Arabia
2
Western Pacific Region
2
Uruguay
2
Turkmenistan
2
Bolivia
2
Papua New Guinea
2
Romania
2
Greece
2
Palestine
2
Central African Republic
2
Poland
2
Angola
2
Bhutan
2
Australia
1
Gambia
1
China
1
Kazakhstan
1
Fiji
1
Singapore
1
Kyrgyzstan
1
Uzbekistan
1
Peru
1
Malaysia
1
Morocco
1
Qatar
1
Bulgaria
1
Guinea
1
Italy
1
USA
1
Guinea-Bissau
1
Lithuania
1
Ireland
1
North America
1
Denmark
1
Maldives
1
Tunisia
1
Côte d’Ivoire / Ivory Coast
1
Djibouti
1
Egypt
1
Yemen
1
Somalia
1
Ecuador
1
Madagascar
1
Authors & Publishers
Publication Years
Category
Countries
1024
Clinical Guidelines
144
Public Health
94
Women & Child Health
74
Key Resources
66
Pharmacy & Technologies
35
Capacity Building
23
Toolboxes
TB
190
HIV
176
Mental Health
89
Pharmacy
78
AMR
78
COVID-19
73
NTDs
56
Conflict
53
Caregiver
39
Refugee
35
NCDs
34
Disability
31
Rapid Response
21
Global Health Education
17
Ebola & Marburg
15
Natural Hazards
13
Planetary Health
10
Specific Hazards
8
Health Financing Toolbox
6
Polio
5
Social Ethics
4
Cholera
3
Zika
3
South Sudan
2
STATUTORY INSTRUMENTS | SUPPLEMENT No. 8 28th March, 2014 | STATUTORY INSTRUMENTS SUPPLEMENT | to The Uganda Gazette No. 18 Volume CVII dated 28th March, 2014 | Printed by UPPC, Entebbe, by Order of the Government. | STATUTORY INSTRUMENTS | 2014 No. 29.
First Revised Edition
March 2000
The Ethiopian Food and Drug Administration (EFDA) is mandated, in the proclamation 661/2009, to ensure the safety, quality and efficacy of medicines. To achieve this, the authority has been working on different regulatory activities. The medicine market authorization system is one of the top priorit...
This was a Phase 3, multi-center, randomized, open-label, parallel-group, active control study where 273 male and female patients with first stage Trypanosoma brucei gambiense HAT were treated at six sites: one trypanosomiasis reference center in Angola, one hospital in South Sudan, and four hospita...
Namibia guideline for submission of applications for registration of pharmaceuticals for human use in common technical document format.
This guideline is intended to provide recommendations to applicants wishing to submit applications for the registration of medicines. It represents the Medicines Control Council’s current thinking on the safety, quality and efficacy of medicines.
These guidelines have been developed to provide guidance to the Ministry of Health in managing applications for registration of human pharmaceutical products in Rwanda. It was compiled by the Technical Working Group (TWG) on Medicines Evaluation and Registration (MER) of the East African Community M...
First edition, November 1997 | Revised July 2002
Procedures Manual - Medicines registration in Madagascar - 2016 version
The Practical manual on laboratory strengthening, 2022 update provides practical guidance on implementation of WHO recommendations and best practices for TB laboratory strengthening. It is an updated version of the GLI Practical Guide to Laboratory Strengthening published in 2017 and provides the la...
This guideline is intended to provide requirements to applicants wishing to submit
applications for registration of medicines in Botswana.
A.55 Medicines and Related Substances Act, 2013 | No. 8 of 2013 | An Act to provide for the registration, regulation of the sale, distribution, importation, exportation, manufacture and dispensing of medicines and related substances, and matters incidental thereto.
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...
