Medical device manufacturing

Bridging design and manufacture - from clinical builds to scale-up

The hardest part of manufacturing isn’t volume, but the transition from design into regulated production. TTP bridges that gap by helping you develop the device and the manufacturing process in parallel, supporting agile clinical and early production builds. With no minimum volumes, no CMO lock-in, and no process IP constraints, you retain control of your product and supply chain. We help you reach the clinic sooner and transfer to full-scale manufacturing with confidence, without late-stage surprises.


Design and manufacturing, tightly integrated

When design and manufacturing work as one team from the start, you avoid the disconnects that often create delays, rework, and transfer headaches later on.

TTP supports you with:

·        Manufacturing input built into design reviews from day one

·        DFM/ DFA insight to make designs production-ready early

·        Faster resolution of build issues through close collaboration

·        Reduced risk at verification and design transfer

·        One continuous journey from prototype to clinical builds

Because we are not a high-volume CMO, our incentives are aligned with yours: to design a process that will scale cleanly when the time is right, not to pull you prematurely into fixed production routes.

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Serac Imaging Systems
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SERac imaging systems
Molecular Imaging at patient bedside with Serac Imaging Systems’ compact hybrid gamma-optical camera
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Job Role

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Achilles Therapeutics
Serac Imaging Systems
Glucotrack
TTP has been an incredible partner, complementing our expertise and delivering designs from whiteboard to moulded functional prototypes. With TTP’s support, Achilles Therapeutics is scaling its manufacturing process and bringing transformative therapies from bench to bedside. The TTP team has shown the same level of excitement as us in getting these therapies to the people who need them.

Ed Samuel

  

EVP Technical Operations

,

Achilles Therapeutics

The team at TTP has done a fantastic job expediting the journey to commercialisation of our prototype. We are excited about the potential for Seracam to improve patients’ lives."

Dr Paul Cload

  

Chief Marketing Officer

,

Serac Imaging Systems

TTP really bridges the gap between true product development and true manufacturing. Their team understands the science, the design trade-offs, and what it takes to bring a novel device into production.

Paul Goode

  

CEO

,

Glucotrack


Rapid builds for clinical momentum

As you approach verification or clinical studies, speed isn’t about rushing, it’s about avoiding months lost to external delays, or slow disconnected teams. Cleanroom and microfabrication capability onsite enables tighter process control for devices incorporating microfluidics, sensors, MEMS-like structures, or precision assemblies, where early manufacturing conditions materially influence performance.

 TTP helps you maintain momentum with:

  • Short lead times for verification and clinical builds
  • Dedicated manufacturing facilities spanning 1,100m², including cleanrooms, microfabrication, assembly, and other specialist labs
  • Faster build–test–refine cycles under one roof
  • Rapid response to engineering changes when designs evolve
  • Controlled builds that generate trusted clinical evidence


No minimums, no forced commitments

Early-stage devices rarely follow predictable demand curves. Manufacturing should flex with your project, not force you into thresholds or long-term commitments.

With TTP, you can:

  • Build singleunits or early series volumes with no minimum order
  • Scale from prototypes to ~100,000 low-complexity devices annually, and hundreds to low thousands for high-complexity systems
  • Support uncertain adoption curves, novel products, or emerging markets
  • Retain full ownership of product and process IP
  • Delay final CMO selection until design maturity, enabling a true competitive bidding process

This gives you strategic freedom: validate the design, mature the process, and then select the right long-term manufacturing partner based on data, not dependency.


Scale-up when you’re ready

The goal isn’t to transfer to a CMO quickly; it’s to transfer at the right moment, with the processes, evidence, and confidence needed to scale smoothly. We can help you with:

  • Manufacturing process development and validation alongside the product
  • Supplier identification and selection informed by hands-on build experience
  • Documentation and data packs to support design transfer
  • Training and collaborative builds with your chosen CMO
  • A smoother pathway from clinical supply to high-volume manufacture

We have successfully transferred programmes to external CMOs following clinical and early commercial builds, with validated processes, qualified suppliers, and clean handovers, reducing the typical friction seen when DfM is theoretical rather than proven in practice.


Regulatory-grade manufacturing confidence

For MedTech, manufacturing isn’t just about making units; it’s about building in a way that stands up to scrutiny. We provide:

  • ISO13485-certified manufacturing where required
  • Full traceability, batch records, and controlled processes
  • Cleanroom environments aligned with medical device standards
  • Evidence that supports verification and clinical builds
  • Access to trusted partners for sterilisation and low-volume fill–finish where needed

How we can help

Clinical builds
New process development and validation
Design integration
DFM/ DFA
ISO 13485 compliance
Complex instrument and device assembly
Filling and sterilisation with our partners
Microfabrication
Manufacturing transfer readiness

Clinical builds

Small-batch manufacture to support verification and clinical studies, delivering controlled builds and traceable data suitable for regulatory scrutiny.

 

New process development and validation

Development and optimisation of manufacturing processes alongside device design, with validation to ensure repeatable, scalable production.

Design integration

Close collaboration between design and manufacturing teams to resolve build challenges early and ensure designs are ready for efficient production.

DFM/ DFA

Design for Manufacture and Assembly insight embedded from the start, reducing complexity, improving build efficiency, and supporting smooth scale-up.

ISO 13485 compliance

Manufacturing within an ISO13485-certified quality system, ensuring full traceability, controlled processes, and compliance with medical device standards.

Complex instrument and device assembly

Assembly of sophisticated electromechanical devices and medical systems requiring precision, specialist processes, and multidisciplinary expertise.

Filling and sterilisation with our partners

Access to trusted partners for sterile fill–finish and sterilisation services, integrated into the manufacturing pathway where required.

Microfabrication

Our in-house microfabrication facility enables fast development of micro-devices, alongside a global network of foundries to allow production transfer of the devices we develop. With processes across silicon, glass and polymers we offer a unique environment to apply the benefits that advanced microfabrication offers in sensors, microfluidics and surface modification technologies.

Manufacturing transfer readiness

Process documentation, supplier selection, and data packages prepared to enable efficient transfer to your chosen high-volume manufacturing partner.

Clinical builds

Small-batch manufacture to support verification and clinical studies, delivering controlled builds and traceable data suitable for regulatory scrutiny.

 

New process development and validation

Development and optimisation of manufacturing processes alongside device design, with validation to ensure repeatable, scalable production.

Design integration

Close collaboration between design and manufacturing teams to resolve build challenges early and ensure designs are ready for efficient production.

DFM/ DFA

Design for Manufacture and Assembly insight embedded from the start, reducing complexity, improving build efficiency, and supporting smooth scale-up.

ISO 13485 compliance

Manufacturing within an ISO13485-certified quality system, ensuring full traceability, controlled processes, and compliance with medical device standards.

Complex instrument and device assembly

Assembly of sophisticated electromechanical devices and medical systems requiring precision, specialist processes, and multidisciplinary expertise.

Filling and sterilisation with our partners

Access to trusted partners for sterile fill–finish and sterilisation services, integrated into the manufacturing pathway where required.

Microfabrication

Our in-house microfabrication facility enables fast development of micro-devices, alongside a global network of foundries to allow production transfer of the devices we develop. With processes across silicon, glass and polymers we offer a unique environment to apply the benefits that advanced microfabrication offers in sensors, microfluidics and surface modification technologies.

Manufacturing transfer readiness

Process documentation, supplier selection, and data packages prepared to enable efficient transfer to your chosen high-volume manufacturing partner.

Speak to one of our experts

Will Cramer

Will Cramer

Will Cramer leads TTP Manufacturing, delivering low to medium volume production of consumables, devices, and instruments to ISO13485 standards. A mechanical engineer with over 25 years’ experience across medical, life science, consumer, and industrial markets, he previously served as VP Engineering and Production at a TTP spin-out. Will holds a master’s in engineering from Cambridge University.

Head of Manufacturing
Fred Hussain

Fred Hussain

Fred leads TTP’s microfabrication capability as part of TTP Manufacturing.He has 30+ years’ experience taking devices from lab toscale-up.Hehas delivered 100+ internal/external projects, mainly in the bio-med sector.​Fred has a Master of Engineering degree in Electronics and a PhD on 3-axissilicon accelerometers.

Sophie Meredith

Sophie Meredith

Sophie is an experienced project leader in TTP’s Biosensing team. She has a PhD in biophysics and has worked on projects involving the development of optical systems, implantable devices, and fluorescence detection for applications in biological sensing

Justin Buckland

Justin Buckland

Multiphysics Analysis and Sensor Development Specialist
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Software capability at TTP

Engages in all stages of software and product development, our software capability at TTP covers the full spectrum–from in-depth analysis and system architecture, to prototype design, implementation and development.

Manufacturing capability at TTP

Working seamlessly with our development teams, we take clients’ products through prototype builds, clinical trials, pilot manufacturing and more. Using TTP Manufacturing reduces uncertainty, risk and time to market for our clients.

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We help clients with all stages of their most complex and challenging technology and product development projects.

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