× Information on this section of ECOLEX comes from the InforMEA Portal which compiled information from MEA Secretariats with the support of the European Union. The accuracy of the information displayed is the responsibility of the originating data source. In case of discrepancy the information as displayed on the respective MEA website prevails. Decision XIII/10: Further study of campaign production of CFCs for metered-dose inhalers (MDIs) Tipo de documento Decision Número de referencia XIII/10 Fecha Oct 16, 2001 FuenteUNEP, InforMEA Estado Activo Materia Desechos y sustancias peligrosas, Aire y atmósfera Tratado Protocolo de Montreal relativo a las sustancias que agotan la capa de ozono (Sep 16, 1987) Reunión Página web ozone.unep.org Resumen The Thirteenth Meeting of the Parties decided in Dec. XIII/10: Noting that the Technology and Economic Assessment Panel and Technical Options Committee review recommended that just-in-time production of CFCs for the manufacture of metered-dose inhalers is the best approach to protect the health of patients, Noting, however, the possibility that just-in-time production of CFCs for the manufacture of CFC-based MDIs may not be available through to the end of the transition, and that the end of just-in-time production could come unexpectedly, To note with appreciation the work of the Technology and Economic Assessment Panel and its Technical Options Committees in studying the issue of campaign production of CFCs for manufacturing CFC-based MDIs; To request the Technology and Economic Assessment Panel and Technical Options Committees to analyse the current essential-use decisions and procedures to identify if changes are needed to facilitate expedient authorization for campaign production, including information needed for the review and authorization of nominations for campaign production quantities, the contingencies for under- and over-estimation of the quantities needed for a campaign production, the timing of the campaign production vis-à-vis export and import of those quantities, the oversight and reporting on the use of campaign production quantities, and the flexibility in ensuring that the campaign production is used only in the manufacture of MDIs for the treatment of asthma and chronic obstructive pulmonary disease or that any excess is destroyed; To request the Technology and Economic Assessment Panel to present its findings to the Open-ended Working Group in 2002; To request the Technology and Economic Assessment Panel to continue to monitor and report on the timing of the likely need for campaign production.