Imagine

Lucid’s experienced team can validate innovative ideas for commercial suitability, market research & understanding, competitor analysis, intellectual property and real-world benefit assessment, utilising a network of medical and clinical specialists.
 
Lucid’s in-house regulatory team can lead you through the regulatory landscape. Fitting within existing regulations can be the difference between instant market availability and years of additional regulatory red-tape.
 
Experienced in all aspects of medical device regulations, we undertake human-factors engineering studies consistent to FDA, CE and UKCA regulatory requirements.

Design

Making the right technology choices is imperative in medical product design. Offering performance, reliability, IPR, health safety and regulatory implications. Let Lucid guide you to make the right technology selection, appropriate for your specific medical device and service requirements.
 
Lucid use human-centered design to focus time, resources, and energy on solutions and innovations that make service delivery effective, easy, and in tune with the emotions of the people using the products and services we design for.

Make

We rapidly prototype and test design iterations involving an expert clinical network.
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We offer manufacturing services from small production batches through to full production delivery.

Our manufacturing capabilities are accredited to the international medical device standard ISO 13485.