Regulatory Customs
Consultancy

Expert regulatory and customs guidance.

From classification and documentation to customs clearance and audit readiness, we navigate international regulations so your shipments move without delay.

Speak to a Specialist

Navigate global compliance with
confidence

Expert regulatory consulting, customs clearance support and GDP-compliant logistics guidance for pharmaceutical, clinical trial, cell & gene and IVF shipments worldwide.

Our consultancy services

Classification &
Documentation

UN3373, PI650, IATA DGR, SDS/MSDS, shipper declarations and compliant labeling for biological materials and Speciality pharmaceuticals.

Country Enablement & Customs

Import Permits, EORI registration, HS classification, Incoterms and country-specific customs requirements.

Packaging Compliance Review

Validation of passive, active and cryogenic packaging solutions for global transport lanes.

Lane Risk Assessment

Route qualification by airport, season, transit duration and temperature profile.

Monitoring & Traceability

Chain-of-custody mapping, temperature logging and audit-ready reporting.

Training & Audit Preparation

GDP/GxP readiness, SOP development, CAPA support and inspection preparation.

Global Customs Expertise

Global Site Support

Managing international shipments requires accurate customs declarations, permits, licensing requirements and country specific regulations. Our experts help you reduce delay, fines and shipment hold.

  • Customs Brokerage Support
  • Import / Export Documentation
  • Permit Management
  • Trade Compliance
  • Regulatory Risk Assessment
  • Cross-border healthcare logistics

FAQ

What is regulatory consulting in pharmaceutical logistics?
Specialist advice on the classification, documentation, permits and customs requirements that govern the international movement of pharmaceutical and life-science shipments.
What regulations does Medair follow for temperature sensitive shipments?
We work to GDP and GxP standards alongside IATA, ADR and country-specific import/export rules for temperature-sensitive and dangerous goods.
Does Medair provide support for OH&S management during transport?
Yes. We advise on the safe handling, packaging and dangerous-goods requirements that keep both product and people protected in transit.
How can I get started with Medair’s regulatory consulting services?
Speak to a specialist and we will review your lanes, products and documentation, then build a compliance plan tailored to your shipments.

Technology that keeps trials moving

GDP
Compliant
Global Regulatory
Guidance
Customs Clearance
Support
Real-Time
Monitoring
Proactive
Alerts
Audit Ready
Documentation
Reporting &
Analytics
24/7 Specialist
Support

Case Study

Emergency Production
Line Recovery

Change after arrival in Sydney. Delivery moved to Queenstown. Nearly 1,200 km additional transport required.

  • 1,197 KM
    Additional distance
  • No Temperature
    excursions
  • 19 hours continued
    driving
View Case Study

Why choose Medair?

Trusted global logistics for
pharmaceutical and clinical shipments.

Discover solutions Request a quote