September 1, 2016

Our Process

Formalised Medical Device
"Conception to Commercialisation Process"

i360medical forms a bridge for new ideas between ALL Healthcare Professionals, Clinicians, Academia, Engineering, Development, Industry and Commercialisation Specialists.

(Pay Per Service)
Develop Innovation Ecosystem
Ideas, Unmet needs
Identification of new ideas
Clinical, Technical and Market Opinions
Clinical Opinions
Client Product Pipelines / Portfolio
IP Portfolio / Transferrable IP
Ideas, Unmet needs
IP Arrangements
Matching prior art with other academic or industry groups
Go no go on ideas with inventors
Ideation support to the inventor
Idea Searches / Sourcing
Initial Design
Initial Design, Proof of Concept, Project Plan
Clinical, Technical and Market Assessment (CTM)
Design, Development and Prototyping, validation verification
RA, CE and FDA 510K initial plan
Design, Development and Clinical Ready Prototyping
Clinical ready product,
Wet Labs (pre-clinical, GLP)
CE and FDA 510K pre approval
IP and Pre clinical, GLP
Design and develop clinical ready product
Complete CE and FDA execution plan
First-in-Man trial
Multisite Market / Regulatory, Clinical Trial
First-in-Man trial project specific
Carried out with international partners
Market Launch with KOLs
CE & FDA Certification
Market, Clinical Training
Pre-sell to industry, exit/partner licensee
Spin Outs, Joint Ventures, Exits