Join Eurofins BioPharma Product Testing and industry specialists for a comprehensive one-day seminar exploring key challenges and solutions in pharmaceutical quality throughout the product lifecycle on the 1st October, DOM Hotel Limburg, Germany.
Designed for quality, analytical, regulatory and manufacturing professionals, this event will provide practical insights into method transfer, stability-indicating methods, dissolution testing, cleaning validation, endotoxin testing and the quality control requirements for complex therapies such as antibody-drug conjugates (ADCs).
Through expert presentations and real-world case studies, attendees will gain valuable knowledge on regulatory expectations, emerging technologies and best practices that support product quality, compliance and patient safety.
What you will learn
- Best practices for pharmaceutical analytical method transfer under GMP
- Key considerations for stability studies and stability-indicating method development
- How to overcome common dissolution and drug release testing challenges
- Modern risk-based approaches to cleaning validation using TOC technology
- Regulatory and technological developments in endotoxin testing
- The latest advances in LAL and recombinant reagent (rCR) testing platforms
- Quality control requirements for antibody-drug conjugates (ADCs)
- Strategies to improve compliance, laboratory efficiency and product quality
- Practical solutions to analytical and microbiological testing challenges
- Emerging technologies supporting pharmaceutical manufacturing and quality assurance
Event Information
Date: 1 October 2026
Time: 9:00 am to 5:00 pm CET
Location: DOM Hotel Limburg, Germany
Cost: Free to attend
Language: English
Talks & Speakers:
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