Pharma / Kühlketten-Modus
Eine GDP-Checkliste für temperaturgeführte Pharma-Luftfracht. Jeder Schritt nennt seine öffentliche Grundlage. Aktive Kühlraum-Kapazität der Airlines wird ehrlich als „nicht verbunden“ gezeigt — niemals erfunden.
+2 °C to +8 °C (refrigerated)
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☐Confirm the product's required range (+2 °C to +8 °C (refrigerated)) and apply the IATA Time & Temperature Sensitive Label.Grundlage: IATA Temperature Control Regulations (TCR) + Time & Temperature Sensitive Label.
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☐Use qualified packaging validated for this lane: active (powered) or passive (insulated + phase-change materials) rated for the transit duration and ambient extremes.Grundlage: EU GDP Guidelines 2013/C 343/01.
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☐Continuous temperature monitoring with a data logger, documented end-to-end (origin → destination), with an excursion SOP.Grundlage: EU GDP Guidelines 2013/C 343/01.
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☐Prefer a CEIV Pharma-certified airline, ground handler and forwarder, with qualified cold facilities at each transit point.Grundlage: IATA CEIV Pharma certification.
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☐GDP-trained personnel for everyone who handles the shipment; qualified storage/transport equipment.Grundlage: EU GDP Guidelines 2013/C 343/01.
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☐Minimise transhipments — every handoff is a temperature-excursion risk. Prefer the most direct routing.Grundlage: EU GDP Guidelines 2013/C 343/01.
Routing & Umladungen
Give origin and destination to see the great-circle distance. Prefer the routing with the fewest transfers (fewer handoffs = lower excursion risk).
TrackJet Geo (own, great-circle) + GDP guidance.
— Kühlkapazität der Airline · not connected
Which airlines currently have active cold rooms / active cold-chain capacity is not connected — verify directly with the airline, or look for IATA CEIV Pharma certification. TrackJet shows no invented capacity.