Medical Devices · Concept to Translational Development

From Concept to Translational Development

We aim to develop next-generation medical devices by integrating biotechnology, nanotechnology, materials science, and digital innovation. Our expertise includes IVDs, biosensors, point-of-care diagnostic devices, nanotechnology-enabled medical devices, wearable health technologies, and smart healthcare solutions — from concept development and prototyping through analytical validation, performance evaluation, regulatory documentation, and commercialisation.

Concept & Strategy Biological Evaluation Preclinical Evaluation Diagnostic & IVD Support Biosensors & PoC Performance Testing Regulatory Documentation
Medical Device Development Support

Eight areas of development expertise

Click any card to explore the full range of services available within each area.

01

Concept Development & Product Strategy

Early-stage scientific definition and strategic planning for medical device concepts.

Feasibility Translational Roadmap
02

Prototype & Proof-of-Concept Support

Scientific evidence generation for evaluating and refining early-stage prototypes.

PoC Studies Design Optimisation
03

Biological Evaluation

Biocompatibility and biological safety studies assessing device and material interactions with biological systems.

Cytotoxicity Biocompatibility
04

Preclinical Evaluation

Safety, biological response, and functional performance evaluation of medical devices.

in vitro Studies Tissue Response
05

Diagnostic & in vitro Diagnostic Device Support

Development and evaluation of diagnostic technologies and IVD solutions.

Assay Development Analytical Performance
06

Biosensors & Point-of-Care Technologies

Support for emerging healthcare technologies integrating biology, sensing, and digital systems.

Biosensors Wearables
07

Medical Device Testing & Performance Evaluation

Scientific and analytical capabilities supporting product characterisation and performance assessment.

Material Characterisation Stability Studies
08

Scientific & Regulatory Documentation Support

Organising scientific evidence and technical documentation for product development and regulatory progression.

Biological Evaluation Docs Technical Dossier
Device Categories We Support

Across the full device spectrum

Diagnostic & IVD devices
Implantable & non-implantable devices
Wound-care products
Drug-delivery devices
Biosensors & wearable technologies
Point-of-care diagnostic systems
Microfluidic devices
Laboratory & research devices
Digital & connected healthcare technologies
Our Development Pathway

Concept to clinical translation

01 →

Concept

02 →

Feasibility

03 →

Prototype

04 →

Proof of Concept

05 →

Biological Evaluation

06 →

Preclinical Validation

07 →

Documentation

08 ✓

Translation