EU Retesting & Batch Release: From Importation to QP Certification
10 Nov, 2026 | 10:30 & 16:30 CEST
Discover how to navigate EU release requirements with confidence. This webinar will discuss the complete pathway to EU batch release, providing practical guidance on importation, GMP testing, QP certification, and accelerating time to market for biologics and advanced therapeutics.
Speakers:
Felix Harion – Scientific Expert, Business Development Manager, Eurofins BioPharma Product Testing Germany
Navigate EU release requirements with confidence
Expanding into Europe requires more than just regulatory approval. Successful market entry depends on the seamless coordination of importation, GMP testing, batch documentation review, and Qualified Person (QP) certification.
Join Eurofins BioPharma Product Testing for an expert-led webinar covering the complete pathway from product importation through analytical testing and final EU batch release. We will discuss practical considerations, common challenges, and proven strategies to accelerate product release while maintaining full regulatory compliance.
Whether you are manufacturing biologics, biosimilars, ADCs, vaccines, peptides, or other advanced therapeutics outside the EU, this webinar will provide valuable insights into the requirements and timelines for entering the European market.
What you will learn
- The role and responsibilities of the Qualified Person during EU batch release
- EU regulatory requirements for product importation, retesting, and QP certification
- Key requirements for documentation review and supply chain qualification
- Importation pathways and GMP expectations for products manufactured outside the EU
- Typical timelines for EU market entry, QC testing, and QP release
- Common causes of delays and how to avoid them
- How integrated QC testing and QP oversight can accelerate market access
Why attend?
Eurofins BioPharma Product Testing provides comprehensive EU product release support through a network of GMP-compliant laboratories and experienced Qualified Persons.
Our end-to-end solutions include:
- QP certification (QP declaration, CoC)
- Analytical method transfer and validation
- Importation and warehousing support
- GMP batch and lot release testing
- Documentation review
- CoA issuance
- OOS investigations
By bringing these services together under one coordinated process, we help pharmaceutical manufacturers reduce complexity, maintain compliance, and accelerate product release.
Gain practical insights from industry experts and learn how to navigate EU retesting, batch release, and QP certification with confidence.
📅 Date: 10 Nov, 2026 | 10:30 & 16:30 CEST