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As a trusted CDMO partner and pharmaceutical packaging manufacturer, Sanner works with biopharmaceutical companies to design, develop, manufacture and package the delivery devices and combination products their therapies depend on, from early feasibility through commercial supply.
We support the biopharmaceutical industry with advanced pharma device solutions and protection systems designed to preserve product integrity and ensure patient safety. We combine regulatory expertise, high-performance materials, and tailored engineering to safeguard highly sensitive therapies.
Leading pharmaceutical companies around the world trust Sanner to deliver. We help biopharma innovators take complex therapies from molecules to patient, even the most difficult-to-deliver formulations.
From the safe handling of high-value, complex biologics, to cell-and-gene therapies, Sanner combines device engineering, drug stability and regulated manufacturing under one roof. Partners stay with us as their programs scale from first clinical builds to full commercial supply.
We have supported hundreds of combination products including autoinjectors, pen injectors, pre-filled syringes, and inhalers, on their path to market.
With experience delivering viscous biologics and difficult-to-deliver therapies, our pre-filled syringe assembly capabilities are backed by decades of hands-on device expertise.
We understand how to preserve volatile chemistry inside combination products and solid oral dose packaging, using pharmaceutical desiccants and advanced moisture management to provide reliable moisture protection across the product lifecycle.
Our global network of ISO Class 7 and 8 cleanrooms ensures flexible small batch and clinical trial manufacturing transitions seamlessly to large-scale production, including drug kitting and drug handling.
Our ISO 13485-certified quality system supports combination products under FDA 21 CFR Part 4, with integrated QMS processes, primary container documentation, and support for relevant eCTD submission sections.
We design packaging with environmental impact in mind from the first concept. We optimize materials to reduce waste across development and production, and help our customers meet their ESG goals without compromising product protection or patient safety.
From development through commercial manufacturing, we help you navigate complex regulatory requirements while ensuring quality, documentation, and validation at every stage.
Robust development of a next generation platform autoinjector.
Resolving reliability failures in an autoinjector delivering an exceptionally high-viscosity biologic.
