Don’t miss our presentations at PODD and CPHI!
- PODD
- Monday, October 27, 2025 – 05:30 PM - 05:45 PM
A Novel Approach to Modelling Injector Performance and Break-Loose Extrusion Force Data
Presenter: Tom Oakley, Springboard, co-presenting with Deep Bhattacharya, Pfizer
- Monday, October 27, 2025 – 05:30 PM - 05:45 PM
- CPHI
- Wednesday, October 29, 2025 – 11:35 AM - 12:05 PM
Rethinking Injector Mechanics – A New Approach to BLEF-Based Modelling
Speakers: Tom Oakley, Springboard, co-presenting with Jay Sayed, Pfizer
- Wednesday, October 29, 2025 – 11:35 AM - 12:05 PM
-
- Wednesday, October 29, 2025 – 12:05 PM - 12:20 PM
Modelling to Market – Enabling Smarter, Faster Injector Development
Speaker: Alex Vasiev, Springboard
- Wednesday, October 29, 2025 – 12:05 PM - 12:20 PM
Meet our experts at the conferences
Feel free to reach out to our sales representatives to arrange a meeting in advance.
Click on the images to send an email.
Design and Develop your Next Clinical Respiratory Device with Sanner
Sanner combines sustainable design, scientific principles and years' of experience designing and delivering respiration drug delivery devices for clients.
Custom Clinical Devices for Respiratory Applications
Develop your next clinical or commercial inhalation device with a team of experts from Sanner. We have experience across a wide range of form factors and delivery methods, from pressurized metered dose inhalers to soft mist inhalers and complex electronic devices.
Find out how more about our expertise and how we have helped clients in the industry.



How We Drive Your Product from Paper to Production

Advanced Modeling Experience
Computational fluid dynamics simulation allows us to model airflow, particle deposition, and spray dynamics with precision before prototyping begins.

Design for Manufacture & Assembly
Our DFMA process aligns functional design intent with scalable production, ensuring consistent device performance from pilot batches through full commercial volumes.

Electromechanical Medical Device Expertise
Today's respiratory devices rely on precise electronics and embedded software to drive delivery mechanisms, monitor performance, and support diagnostic functions.
Sanner Accelerates Development for Clinical Respiratory Devices
Design & Development
-
Human Factors
-
Industrial Design
-
Device Engineering
-
Electronics and Software
-
Regulatory Services
Scalable Manufacturing
-
Design for Manufacture
-
Cleanroom Injection Molding
-
Class 7 & 8 Cleanrooms
-
Small Batch and Clinical Builds
-
Commercialization

Manufacturing medical devices for use in clinical trials
Clinical trials are an inherent step in the development process for a device. However, manufacturing devices for clinical trials can be a challenge. Find out how we helped PulmoBioMed with their device development and manufacture.
Delivering and maintaining optimal DPI performance
In this whitepaper, Chris Gilmor looks into the demand and device development challenges for DPI's including how to handle moisture. He looks into how to maintain performance without compromising the formulation and tackles environmental moisture challenges for the devices.


Developing a Simpler Nasal Vaccine Administration Device for Infants
The quicker a vaccine is administered to infants, the better, for the parents and patients alike.
A leading vaccine supplier approached Sanner to design and develop a device that enabled faster nasal administration for their vaccine, reducing user steps, to get the right dose for the child.
Shielded Therapeutics: Could Polymeric Nanoparticles Safeguard Inhaled Drugs?
Polymeric nanoparticles (PNPs) represent a groundbreaking advancement at the cutting edge of pulmonary drug delivery, holding great promise for overcoming the key challenges in respiratory medicine.
Find out some key finding in this field and the opportunities and challenges that come with it.

Worldwide production capacity and device development services
Sanner operates a global manufacturing network with a total production space of 28,500 sqm, including 11,000 sqm of cleanroom space (Class 7/8). Our Design Centers of Excellence, Springboard and Gilero, are strategically located in the UK and across the US. Our manufacturing facilities are based in the US, Asia and Europe.
How we can help you
- Capacity for small-batch prototypes and scaling to full production. Our facilities are equipped to handle a wide range of production needs:
- High precision fully electric thermoplastic injection molding capable of handling small shot weights (around 0.1g) up to 64-cavity molds (max. 350T), including 2K molding with thermoplastic elastomers (TPE).
- Manual assembly up to fully automated assembly processes, incorporating mechatronic components for enhanced efficiency and precision.
- End of line packaging for sub-assemblies or finished goods
- Sterilization through trusted external partners, utilizing validated processes to ensure compliance with industry standards.
- Our experience in successfully transferring innovations to production across the EU, US, and China speaks to our ability to bring cutting-edge technologies to global markets. All phases of device development can be supported from our Design and Development Centers of Excellence in both the US and EU.
- Our design transfer processes enable the smoother path to market. We offer end-to-end thinking from development to manufacturing all under one roof to de-risk your project and for a better time to market.
- Our reliability and collaborative working attitude support you in any stage of your project.
Quality control processes and compliance with ISO 13485
Sanner Group facilities are ISO 13485 certified for Design & Development and Manufacturing respectively. Over 250 ISO, AAMI/ANSI standards are used routinely. Our streamlined quality system satisfies the FDA requirements for both the device quality system regulations and the part 210/211 cGMP regulations.













