Filter
715
Text search:
drug
manufacturing
Featured
59
189
Language
Document type
368
132
119
34
34
10
9
3
3
2
1
Countries / Regions
36
31
30
20
20
19
19
13
13
12
12
12
12
12
9
9
8
8
8
8
8
7
7
7
6
6
6
5
5
4
3
3
3
3
3
3
3
3
2
2
2
2
2
2
2
2
2
2
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
1
Authors & Publishers
Publication Years
Category
298
57
31
29
16
13
4
Toolboxes
84
81
53
47
37
34
16
14
14
13
12
11
9
5
5
4
3
3
2
1
1
1
This guideline is intended to provide requirements to applicants wishing to submit
applications for registration of medicines in Botswana.
First edition, November 1997 | Revised July 2002
Made under Section 5 (c) of the Tanzania Food, Drugs and Cosmetics Act, 2003 | Second Edition
• provide scientific information on the safety, efficacy, and quality control/ quality assurance of widely used medicinal plants, in order to facilitate their appropriate use in Member States;
• provide models to assist Member States in developing their own mono- graphs or formularies for these
...
The MSF qualification scheme is concerned with the pharmaceutical quality assessment for drugs. This procedure is applicable to products for international supply, i.e. products supplied through the MSF procurement centres. This qualification procedure is not applicable for local purchase, i.e. purch
...
