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Model Guidelines for the International Provision of Controlled Medicines for Emergency Medical Care
(1996; 14 pages) [French] Voir le document au format PDF
Table des matières
Afficher le documentLIST OF CONTRIBUTORS TO THIS DOCUMENT
Afficher le documentI. INTRODUCTION
Afficher le documentII. DEFINITIONS
Afficher le documentIII. PURPOSE AND PRINCIPLE
Afficher le documentIV. SCOPE OF APPLICATION
Afficher le documentV. SELECTION OF SUPPLIERS
Afficher le documentVI. OUTLINE OF STANDARD AGREEMENT BETWEEN SUPPLIERS1 AND CONTROL AUTHORITIES OF EXPORTING COUNTRIES
Afficher le documentVII. SUMMARY OF THE REQUEST PROCEDURE
Afficher le documentAnnex 1
Afficher le documentAnnex 2
 

V. SELECTION OF SUPPLIERS

Suppliers should be limited to those recognized by the control authorities of exporting countries. They should at least have:

(1) adequate experience as a supplier of good quality emergency medical supplies

(2) managerial capability to assess the appropriateness of requests for the simplified procedure from operators

(3) adequate level of stock and a responsible pharmacist

(4) sufficient knowledge about the relevant international conventions

(5) standard agreement with the control authorities of exporting countries (see section VI below)

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