- Expertise and Innovation
At Eurofins, we are at the forefront of pharmaceutical quality control and testing. Our team of experts will be on hand to share insights into our cutting-edge services and solutions that ensure the highest standards of safety, efficacy, quality and compliance.
- Exclusive Presentations
Attend our exclusive presentations where our specialists will discuss the latest advancements in pharmaceutical testing, including new methodologies, technologies, and regulatory requirements. Gain valuable knowledge that can help streamline your processes and enhance your product quality. More information will follow soon.
- Networking Opportunities
PharmaLab Congress is a prime opportunity to network with industry leaders, professionals, and peers. Meet with our team to discuss your specific needs, challenges, and how Eurofins can support your goals. Forge valuable connections and explore potential collaborations.
- Personalised Consultations
Schedule a one-on-one consultation with our experts to receive personalised advice and solutions for your unique challenges. Whether you're looking to optimise your testing processes, comply with stringent regulations, or enhance your product quality, we are here to help.
About Eurofins BioPharma Product Testing:
Eurofins BioPharma Product Testing is the largest network of harmonized bio/pharmaceutical GMP product testing laboratories worldwide providing comprehensive laboratory services for the world's largest pharmaceutical, biopharmaceutical and medical device companies.
Our service offerings are fully comprehensive and include testing of drug substance, final product, intermediates, and starting materials for both small and large molecule drug products.
We give clients the flexibility to choose from three service models to meet specific project needs, including the award-winning PSS Insourcing Solutions® and we also provide secure 24-hour data access via our online data portal, LabAccess.comSM.
Our laboratories offer a broad range of methodologies under GMP authorization, ISO 17025 accreditation and ISO 9000 certification and all analysis are performed according to European and British Pharmacopeia (EP and BP), United States Pharmacopeia (USP) and Japanese Pharmacopeia (JP), as well as specific customer methods.
With a global capacity of more than 200,000 square meters and facilities located in Australia, Belgium, Canada, Czech Republic, Denmark, France, Germany, India, Ireland, Italy, Japan, Netherlands, New Zealand, Slovakia, Spain, Sweden, Switzerland, UK and the US, our network of GMP laboratories operates under the same strict quality procedures, LIMS and centralized billing system across more than 45 locations worldwide.
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