EU & UK Customs Clearance
Cross border pharmaceutical logistics demands precision, regulatory accuracy, and flawless documentation. Delays, errors, or incomplete filings can compromise temperature stability, increase risk, and impact patient safety.
Pharma Premier eliminates those risks by managing all customs requirements in-house, ensuring documents, declarations, and transit procedures are aligned with transport plans and temperature-controlled movements.
Everything — from import declarations to GVMS entries are handled by trained specialists working directly alongside our GDP operations team.
Capabilites
-
Real-time Electronic Customs Declarations
-
Import, export, and transit clearances (UK/EU) (T1/T2)
-
MHRA, HMRC, and EU authority compliance
-
Controlled substance routing and paperwork
-
ENS/EXS/GVMS/PBN submissions
-
CS2 and security compliance
-
Global network
Key Benefits
-
Single Point of Accountability
-
In-house processing ensures documentation matches transport data.
-
Reduced Risk of Delay or Error
-
Temperature Protection Through Fast, accurate customs processing
-
Every declaration, clearance, and transit document is logged, monitored, and available for QA review.
-
Full Regulatory Alignment
-
Seamless Integration with GDP Transport
Ideal for
-
Clinical trial shipments
-
High-value pharmaceutical consignments
-
Controlled drugs and special category medicines
-
Temperate and frozen biologics
-
Diagnostic kits and laboratory samples
-
Time-critical commercial distribution
Pharmaceutical shipments cannot tolerate administrative delays. Incorrect data, missing declarations, or poorly executed transit procedures can:
-
stall vehicles at borders
-
expose products to temperature risk
-
disrupt clinical trial timelines
-
increase cost and regulatory exposure
Pharma Premier’s in-house customs team ensures the fastest, cleanest, and most compliant route through UK/EU borders, protecting both product integrity and patient safety.