Here is a sobering fact: Between 2018 and 2023, the FDA issued more than 260 warning letters, recalling over 700 products between 2012 and 2021 alone, all due to issues linked to stability studies.
Every day your product is delayed, your path to market slows. Stability studies are a regulatory requirement, but with guidelines difficult to interpret or implement for many manufacturers, as well as expensive protocols and costly delays at stake, they can quickly become a source of frustration and risk, particularly for patients.
Whether you're launching a new drug or managing lifecycle support, ensuring the long-term safety, efficacy, and quality of your product is non-negotiable.
The Eurofins BioPharma Product Testing (BPT) network of laboratories provides expert support across the entire lifecycle of your stability programme – from method development to analysis, storage, and reporting – helping you meet international regulatory standards including ICH Q1(A), ICH Q5C, and VICH GL3.
Our GMP-compliant facilities offer:
With secure, monitored climatic chambers, your samples remain safe at all times, with sample storage for both short- and long-term needs.
Our expert teams will work with you to optimise your study design, helping to reduce costs while ensuring compliance. If your study was conducted in-house, we can assist in interpreting results or continuing analysis using the same protocols.
Whether you’re conducting early-phase studies or preparing for submission, we ensure a seamless experience with rapid setup and data access. Our tailored services help you stay agile, avoid regulatory pitfalls, and focus on what matters—getting your product to patients safely and efficiently.
Our clients trust Eurofins BPT to deliver stability studies that remove uncertainty and help them make the right decisions faster.