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DRUGS REGULATORY UNIT | NOVEMBER 2009 | SECOND EDITION
Drug Advisory Board
Accessed November 2017.
Act 851 | AN ACT to revise and consolidate the law relating to public health to
prevent disease, promote, safeguard, maintain and protect the health
of humans and animals and to provide for related matters.
Expert opinion of the European Tuberculosis Laboratory Initiative core group members for the WHO European Region.
Namibia guideline for submission of applications for registration of pharmaceuticals for human use in common technical document format.
Guidance for the preparation and submission of dossiers
The Zimbabwe National Pharmacovigilance Policy Handbook, 2nd Edition updates the November 2013 version to indicate the Zimbabwe National Pharmacovigilance (PV) Centre’s compliance with the WHO Pharmacovigilance Indicators Handbook 2015.
WHO/CDS/TB/99.272
Distr.: General, Original: French
