Medical devices (EU MDR 2017/745): surgical instruments, diagnostic systems, protective equipment. Pharmaceutical products: +2C to +8C for biologics and vaccines, +15C to +25C controlled room temperature for general pharma. Laboratory reagents and diagnostic test kits. Shipments from Germany (Berlin, Frankfurt, Munich), the Netherlands (Amsterdam), and Switzerland (Basel) to Latvian hospitals, clinics, and pharmaceutical importers.
EU GDP guideline (2013/C 343/01) requires documented cold chain, calibrated instruments, and deviation protocols. Each shipment includes temperature loggers with exportable data records. Transport procedures follow GDP qualification requirements: carrier qualification, deviation management, and insulation standards. Pharmaceutical imports require CE/MDR declaration of conformity, import authorization, and certificate of analysis (CoA). Urgent cases are served with expedited customs clearance and express routing from Germany within 2 days.
Core lane: Germany to Latvia, 2 days, FTL or LTL. Netherlands, Belgium, Switzerland to Latvia with consolidation. Export: Latvia to Lithuania (Vilnius), Estonia (Tallinn), Poland (Warsaw). Documents: CMR with temperature annex, CE certificate, declaration of conformity, import license, CoA for pharmaceuticals. For pharmaceutical transport, carrier WDA (Wholesale Distribution Authorisation) may be required depending on the importer's license conditions.
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Answers to frequently asked questions
GDP (Good Distribution Practice) is an EU guideline for pharmaceutical product distribution. It requires documented cold chain, calibrated instruments, and deviation protocols. For medical devices the key requirements are MDR compliance and CE marking.
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