The New Emergency Health Kit 98: Drugs and Medical Supplies for 10,000 People for Approximately 3 Months
(1998; 82 pages) [French] [Spanish] View the PDF document
Table of Contents
View the documentAcknowledgments
View the documentIntroduction
Open this folder and view contentsChapter 1: Essential drugs and supplies in emergency situations
Open this folder and view contentsChapter 2: Comments on the selection of drugs, medical supplies and equipment included in the kit
Open this folder and view contentsChapter 3: Composition of the New Emergency Health Kit 98
View the documentAnnex 1: Basic unit: treatment guidelines
Open this folder and view contentsAnnex 2: Assessment and treatment of diarrhoea
Open this folder and view contentsAnnex 3: Management of the child with cough or difficult breathing
View the documentAnnex 4: Sample data collection forms
View the documentAnnex 5: Sample health card
Open this folder and view contentsAnnex 6: Guidelines for suppliers
Open this folder and view contentsAnnex 7: Other kits for emergency situations
Open this folder and view contentsAnnex 8: Guidelines for Drug Donations48
Close this folderAnnex 9: Model Guidelines for the International Provision of Controlled Medicines for Emergency Medical Care52
View the documentIntroduction
View the documentDefinitions
View the documentPurpose and principle
View the documentScope of application
View the documentSelection of suppliers
View the documentOutline of standard agreement between suppliers53 and control authorities of exporting countries
View the documentSummary of the request procedure
View the documentModel shipment request/notification form for emergency supplies of controlled substances
Open this folder and view contentsAnnex 10: References
View the documentAnnex 11: Useful addresses
View the documentOrganizations which have collaborated in the preparation of the New Emergency Health Kit 98
View the documentBack Cover
 

Summary of the request procedure

(1) Operator’s role

The operator should make a written request for emergency supplies of controlled substances to the supplier, using the attached model form. The operator is responsible for:

• information provided on the form;

• actual handling of controlled drugs at the receiving end or adequate delivery to the reliable recipient;

• reporting to the control authorities of the receiving country (whenever they are available) as soon as possible;

• reporting to the control authorities of the receiving country on unused quantities, if any, when the operator is the end-user or to arrange for the end-user to do so;

• reporting to the control authorities of the exporting country through the supplier, with copy to the INCB, any problems encountered in the working of emergency deliveries.

(2) Supplier’s role

Before responding to the request from the operator, the supplier should be convinced that the nature of the emergency justifies the application of the simplified procedure without export/import authorizations. The supplier is also responsible for:

• submitting immediately a copy of the shipment request to the control authorities of the exporting country;

• submitting an annual report on emergency deliveries and quantities of drugs involved as well as their destinations, with copy to the INCB;

• reporting to the control authorities of the exporting country, with copy to the INCB, any problems encountered in the working of emergency deliveries.

(3) Control authorities’ role

The control authorities of the exporting country should inform their counterpart in the receiving country (whenever they are available) of the emergency deliveries.

The control authorities of the receiving country have the right to refuse the importation of such deliveries. Emergency deliveries need not be included in the estimate of the receiving country, since they are regarded as having been consumed in the exporting country.

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Last updated: May 3, 2013