With Camgenium, the Prototype phase is a slingshot to accelerate your product to market

Clinician is briefing a patient about an upcoming procedure.  The clinician has developed the app so that it contains the information the patient needs to know to be able to give informed consent for the procedure
Camgenium accelerates and systematically de-risks development of medical device grade prototypes. This image shows a patient consenting app being updated to have additional information that the patient can refer to at home. This information includes questionnaires to fill in before coming to hospital for a procedure.

Initial revenues and first mover advantage are crucial

We aim to get your product completed, certified and in use as quickly as possible to maximise your first mover advantage and bring forward revenues.

The prototype phase is a critical part of Camgenium's process. We work closely with you to deliver and deploy your product in the least time, minimising your risk and ensuring regulatory compliance

Camgenium’s platform rapidly creates prototypes to full medical device standards, so commercial and product / clinical trial activities can start during this phase

Dr Philip Gaffney OBE

CEO

Our approach is supported by two key pillars:

Medical device platform

Don't reinvent the wheel!

The key advantage of building your prototype on the Camgenium platform is quite simply the amount of tested and proven functionality it brings to your product.

It has a massive feature set that covers most common components of software medical devices, and it brings truly sophisticated and richly featured technology to connect hardware medical devices to the cloud.

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Project methodology

Bring forward tasks to shorten timescales

At Camgenium we develop as many of the project components in parallel as possible. Using our platform greatly reduces the usual risks of parallel development and minimises timescales due to its extensive tested and verified feature set.

We also plan for as much trial and evidence capture as possible during prototyping to shorten the time needed for final clinical trials, the last stage before your product can be certified for development.

Our compliance management tools make this possible.

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Innovators are driven by the desire to make a difference - as soon as possible! We share your passion.

Jane Aldridge

CFO

We are with you. We support you and reduce your regulatory risks throughout the whole lifecycle.