Store cartons, VIP assemblies and PCM components in a clean, seco, controlled area. Antes de usar, verify the system size and seasonal configuration, then inspect every VIP for punctures, cortes, crushed edges or loss of rigidity. Do not use a damaged panel.
Condition each PCM component according to the approved standard operating procedure. Control and record the required time, temperature and any tempering step; visual appearance alone does not confirm readiness.
Assemble the documented configuration. Keep PCM orientation, autorización de carga útil, carga mínima y máxima, contención secundaria, cushioning and data-logger position consistent with the tested packout. Prevent direct contact between very cold components and freeze-sensitive medicines unless specifically approved.
Close and seal the carton, record component lots, pack time and logger ID, and apply the required healthcare or dangerous-goods marks. Performance depends on the complete configuration, carga útil, acondicionamiento, perfil ambiental y manejo. Qualify representative loads before routine use and manage changes through the buyer's quality system.