EU Test & Release
Regulatory-Compliant Batch Testing & Certification for the European Market
Expanding into the European pharmaceutical market requires strict adherence to EU Good Manufacturing Practice (GMP) regulations. At Frontier Zdravlje, we offer comprehensive EU test and release services to ensure your pharmaceutical products meet all regulatory requirements for market entry.
Why Choose Our EU Test & Release Services?
EU GMP-Certified Facilities – Fully compliant testing and batch release processes in accordance with EMA guidelines.
Qualified Person (QP) Release – Expert QPs oversee and certify each batch for legal distribution in the EU.
Comprehensive Analytical Testing – Stability, microbiology, and chemical analysis for full regulatory compliance.
Fast & Efficient Turnaround – Streamlined processes to minimize delays and accelerate market access.
Seamless Import & Regulatory Support – Assistance with importation, documentation, and compliance for non-EU manufacturers.
Our Services Include:
Batch Testing & Certification – Full analytical and quality testing to confirm compliance with EU regulations.
Qualified Person (QP) Batch Release – QP oversight to certify products before distribution.
Regulatory Support & Documentation – Ensuring all required records, CoAs, and compliance reports are in place.
Storage & Distribution – Warehousing options for smooth logistics within the EU market.
Our Offerings
View our other offerings
Get In Touch
Streamline Your Supply Chain with Zdravlje
With our pharmaceutical-grade warehousing services, we ensure your materials are stored and managed with precision.
Get in touch today to learn how we can support your storage and logistics needs.