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Technical assitance in drug policies

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Pan American Health Organization World Health Organization

XV

XVII! Regiona

I!

Pan

A

merican

S

anitary

Conference

l

Committee

M

eeting

Washington, D. C., U.S.A. September-October _966

I ii I

CSP17/31 (Eng.)

22 September 1966 ORIGINAL: SPANISH

TECHNICAL ASSISTANCE IN DRUG. POLICIES

Item proposed by the Government of Chile

There is no doubt that medicaments is a major item in the cost of health activities of which they are an indispensable tool, and that these activities continue to be urgently needed in the Hemisphere. Advances in

this field are so great that it is very difficult at the present time for

drugs to be produced except by large-scale undertakings. On the other hand, the industrial concerns producing generic drugs and pharmaceutical preparations usually multiply their products, for obvious reasons, and thereby create commercial situations in which the countries have diffi -culties in obtaining at a reasonable price a supply of drugs which are adequate in quantity and quality.

Both WHO and PAHO in the Hemisphere have been actively and usefully concerning themselves with various aspects of the drug problem, which activities have been stimulated by the present authorities of the

Organi-zation. However, this collaboration should be given greater stimulus, and greater scope _ and should include assistance in obtaining an appropriate and socially advisable supply° Hence,the Government of Chile considers it advisable to present the following

RESOLUTION:

To congratulate the Organization on its activities aimed at stimulating and improving the control of medicaments and on the assistance it is giving in organizing laboratories for the quality control of medicaments ;

To request the Director of the Bureau to examine, by appro -priate means, the problem of the supply of generic drugs and

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CSP17/31 (Eng.) Page 2

To request the Director to service the requests for technical assistance submitted by Member Countries for standardizing their present systems for the supply and control of medicaments;

To request the Director of the Bureau to establish machinery for informing Member Governments about matters of drug policy and regulation; on new products of proven utility; and, in general, on progress in theoretical and applied pharmacology;

To recommend that appropriate machinery be established in this field to ensure the coordination of the activities of the Organi-zation in this field and those of international and government

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