MK Pharma

Protecting every degree that matters. End-to-end pharmaceutical handling with defined temperature bands, qualified processes, and clear visibility—because patient safety begins with shipment integrity.

Why MK Pharma

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Tight Temperature Control Defined ranges and qualified storage/transfer.

Time-Critical Flow Prioritized cut-offs and quick tarmac moves.

Proven SOPs Pharma-specific acceptance, handling, and exception control.

Expert Support Teams trained for pharma documentation and audits.

Network Confidence Established lanes and hub capability for health logistics.

Typical Shipments Finished medicines and vaccines Clinical trial materials APIs and intermediates (non-haz) Biologics within declared ranges Note: DG-classified pharma follows DGR rules; dry ice declared per package.

Certifications & Standards GDP-aligned SOPs and audits IATA CEIV Pharma (where applicable; list stations) IATA PCR compliance and validated equipment flows

Requirements Docs: CI, packing list, AWB; temp declaration; any permits Packaging: Qualified active/passive systems; dry ice (UN1845) weight per piece/ULD Pre-Alerts: Routing, logger use, special handling codes

Options Temperature Bands (e.g., +15–25°C, +2–8°C, frozen) Priority Handling for shorter ground times Enhanced Visibility (event alerts; shipper loggers) Hub Services: re-ice/re-pack where available

Frequently Asked Questions

Yes—within station capability and declared packaging performance. We’ll confirm at booking.

Bring your own; we’ll accept and keep with the shipment.

We escalate per SOP with documented actions and notifications.

Talk to our team → maskargo.com/support/contact-us/ MASkargo — Keeps Business Moving.