As an innovation-driven pharmaceutical manufacturing partner, Sanner supports combination product development from first concept through commercial launch. We transform your ideas into market-ready drug delivery devices and drug delivery packaging with early-stage design and concept development services. Our solutions are purpose-built for manufacturability, regulatory compliance, and scalable production.
We blend user-centered design with engineering rigor to ensure clinical effectiveness, technical feasibility and regulatory compliance, developing pharmaceutical delivery systems that take your device from paper to production.
Our team of experienced experts spans science, engineering, and manufacturing expertise.
Whether your device is in development or already on the market, we can help you analyze risks, overcome challenges, minimize threats, speed up launch, and reduce cost.
Contact us to discuss your next autoinjector, pen injector, or on-body delivery system.
Optimal manufacturing processes are a key component to market success, and we are rigorous in our quality management processes and adhere to ISO 13485 regulatory controls.
We strive for user preference even for the most complex indications and difficult-to-deliver therapies such as viscous biologics and cell-and-gene therapies. Projects follow a human-centered approach to ensure that patients, healthcare professionals and carers find the devices safe, effective, and even enjoyable to use.
With experts in fluid mechanics, materials science, engineering design, and other scientific disciplines, the team has the knowledge required to fully understand the mechanisms of your device, from scientific principles, such as aerosol performance, to autoinjectors for the most viscous drugs.
Robust development of a next generation platform autoinjector.
Accelerating the time to market for a novel ophthalmic implant drug.
Developing a connected syringe accessory that makes the smallest doses measurable.
