E-DRUG: Role of DRA in NDP implementation
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Dear e-drug community
In relation to a current work assignment in Ethiopia I am interested to
learn about other countries' experiences/set-ups regarding the roles and
responsibilities of the drug regulatory authority (DRA) versus the Ministry
of Health in relation to National Drug Policy (NDP) development and
implementation.
In Ethiopia (and (previously?) Uganda) the DRA is charged with all NDP
development and implementation related activities, while many other
countries have a set-up where legislation enforcement is the responsibility
of the DRA, while policy development and implementation planning and
monitoring remains under the MOH.
I would appreciate if e-druggers could provide feed-back on the prevailing
set-up in their respective countries, and on possible strengths and
weaknesses of both systems.
Thanks in advance
Marianne
Marianne Schurmann
Pharmaceutical Consultant
Spain
e-mail: eschurmann@icam.es